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Key evidence withheld as 'trade secret' in EU's controversial risk assessment of glyphosate

Companies who make the pesticide glyphosate refuse to disclose key scientific evidence about its possible risks in the name of trade secrets protection. CEO appeals to the European Food Safety Authority (EFSA) to disclose all the possible original elements of three key scientific studies it used in assessing glyphosate as “unlikely” to cause cancer to humans. We also call MEPs to reject the Trade Secrets Directive in the April 2016 plenary vote on the final text.

In March 2015 the World Health Organisation's International Agency for Research against Cancer (IARC) found the world's most commonly used herbicide, glyphosate, “probably carcinogenic to humans”. Three months later the EU's official risk assessment of the pesticide, conducted by the European Food Safety Authority (EFSA) and Germany's Federal Risk Assessment Institute (BfR), came to the opposite conclusion that glyphosate was “unlikely” to cause cancer to humans. A war of words started with, notably, EFSA's director calling scientists critical of its work (including some involved in IARC's review) “facebook scientists” for a petition they had sent to the European Commission... And it continues with, lately, directors of the two organisations engaging in a public exchange of letters, copied to more or less everyone politically involved on this file,1 where both defended the integrity of their respective institution's work. Eventually, a meeting between the two, meant to take place this week, was cancelled, as EFSA did not agree to the IARC's director's requests to change a number of its statements about IARC's work on its website.

One reason behind this almighty mess is the extreme public sensitivity of the topic: behind glyphosate lurks the shadow of US multinational Monsanto, currently one of the most hated companies on the planet, which built its economic development around this wide-spectrum herbicide and GM crops engineered to tolerate it. Monsanto coordinated industry producers into a Glyphosate Task Force (GTF) to facilitate the pesticide's review approval.

But the story has more to it than a political tussle. While conflicts are common in science too, resolving them relies on scientists reviewing and debating the evidence. The problem is this step cannot be taken because parts of this evidence are missing. Three industry-sponsored carcinogenicity studies on mice, in particular, are not accessible to IARC while EFSA insists they played an important role in informing its decision. This situation is unfortunately typical of debates on pesticides regulation.

This is why for years Corporate Europe Observatory and others have been asking EFSA and the European Commission that, just as with clinical trials for medicines, the data supporting EFSA's scientific opinions should systematically be made public to enable free scientific scrutiny. To find out more about the basis of the glyphosate decision in December 2015 we filed an access to documents request to EFSA to demand the disclosure of these three mouse studies.

EFSA refused, and justified this on the basis that the owners of the studies, all industry producers of glyphosate, said disclosing this evidence would undermine trade secrets and intellectual property rights. Corporate Europe Observatory is appealing that decision by EFSA.

Meanwhile, the political process goes on, with the European Commission expected (according to EU sources) to propose member states start discussing a new EU-wide renewal of glyphosate's market authorisation next March 7-8. To add to the tension, France's food safety agency ANSES published on 12 February an opinion contradicting EFSA's (even though ANSES officials had contributed to it) by saying that glyphosate could perhaps, after all, be classified2 as a substance suspected of being carcinogenic to humans – a category which would not imply an EU ban – and that more research should be done, in particular by the European Chemicals Agency (ECHA) in Helsinki.

The Mysterious Three

The starkest difference between the EU's regulatory agencies and the independent scientists who wrote IARC's assessment perhaps lies in their respective interpretation of the animal evidence. The conflict is particularly intense over the EU's use of five industry-sponsored carcinogenicity studies in mice reviewed by BfR and EFSA. Two of these studies, from 1983 (“A chronic feeding study of glyphosate (Roundup technical) in mice 77-2061! (BDN-77-420)”) and 1993 (“Glyphosate: 104-week dietary carcinogenicity study in mice, IRI 438618”), were already included in industry's first EU level request for a market authorisation for glyphosate. But industry sent three new unpublished studies for the EU market authorisation renewal (the “Mysterious Three”, as scientific literature reviews specialist Paul Whaley dubbed them) :

- “Carcinogenicity Study with Glyphosate Technical in Swiss Albino Mice” (2001), following OECD Guideline 451 & GLP – study owned by the Israeli pesticides company ADAMA Agan Ltd and was never published;

- “Glyphosate technical: Dietary Carcinogenicity Study in the Mouse” (2009), following OECD Guideline 451 & GLP – study owned by the Australian pesticides company Nufarm and was never published;

- “HR-001: 18-Month Oral Oncogenicity Study in Mice” (1997), following following OECD Guideline 451 & GLP – study owned by the Japanese pesticides company Arysta LifeSciences Corporation and was never published.

The dangerous life of Monsanto employees

The names of the authors of all five studies are redacted in EFSA's publications. In a Twitter exchange on the matter, Monsanto Europe explained this was for security reasons: “If you get scientists' names what's stopping people going after them/families?” The company later added to its first reply saying: “It's a sad fact that some activists target Monsanto employees for harassment,” but this seems simply irrelevant in this case given that not a single Monsanto employee seems to have been involved in the conduct of these studies.

Despite the first two studies, from 1983 and 1993, also not having been published, IARC could access3 them. Indeed it interpreted the 1983 study as showing “a significant increase in the incidence of rare tumours, with a dose-related trend, which could be attributed to glyphosate”, in stark contrast with EFSA and BfR's review of the same study. IARC's interpretation of the 1993 study is on the other hand consistent with EFSA and BfR's. But it could not evaluate the three more recent studies, even though it was able to access summaries which its scientists commented showed incidence of various tumours.

“Key” and “pivotal” evidence

The Mysterious Three are an essential element of the conflict. This is particularly so because EFSA heavily referred to them to explain its assessment, with José Tarazona, the Head of EFSA's Pesticides Unit in charge of the assessment, calling them “key” and “pivotal”. Similar comments can be found from various member states' experts,4 with Belgium insisting that “it was unfortunate that IARC did not take into account 3 guideline studies in both mice and rats, since this could have put the overall conclusions in another perspective”. This very unfair sentiment (IARC could not access these studies) was echoed by Ireland: “IARC's failure to evaluate the 3 other studies is not helpful.”

Since EFSA's publication, the agency has been arguing that there is enough detailed information in its documentation to perform a good analysis, but IARC scientists respond that the descriptions and summaries published miss key elements and cannot replace original data. Among these missing elements, IARC said,5 are "the historical control data from the reporting laboratory for all tumours with statistically significant positive increases, by either test recommended by OECD; another is the survival of the animals". More generally, IARC pointed to its list of attention points for all studies it assesses. [18 February 2016 addition]

Secret perfection or convenient argument?

So what is in these Mysterious Three? How can only three studies explain such a striking contrast? Would they be so strong as to convince IARC to reverse its stance? Would they on the contrary confirm it? Or, given the strong political interest in this file and the fact that the EU's Pesticides Regulation would force glyphosate out of the market were its cancer-causing properties confirmed, isn't referring to these secret studies a convenient argument for all those willing to keep glyphosate on the EU market anyway?

In its response to Corporate Europe Observatory on 5 February 2015 explaining why it would not release the information, EFSA said that the studies' owners (who, by law, must be consulted) refused any disclosure because they considered their studies to contain trade secrets and intellectual property which if released would harm their industrial and commercial interests as well as their “competitive position”. EFSA agreed with this analysis and explained that, according to the exception foreseen in the EU's Public Access to Documents Regulation 1049/2001 as well as in the EU's Pesticides Regulation 1107/2009, it was entitled to not disclose the documents.

Abusive use of the trade secrets protection argument

However, both regulations only protect commercial interests and, in the case of the Pesticides Regulation, a limited list of elements within the studies, not the whole document – it is difficult to believe that everything in a scientific study would be a trade secret. Moreover, the EU's Pesticides Regulation stipulates that any data owner refusing disclosure of its material must provide a verifiable proof that disclosure would harm him, which was apparently not done. Finally, glyphosate has been off-patent for 15 years and most pesticide companies now producing glyphosate belong to the Monsanto-led Glyphosate Task Force, the group that bundled all these studies together and sent them to the BfR and EFSA: how would disclosing these studies harm any of these companies' competitive position if they were already shared among the main competitors?

As a consequence, CEO is appealing this decision, hoping that EFSA will use the opportunity of this major file and controversy to demonstrate its good faith in actually acting upon its declared intentions on data transparency and providing a level of openness that enables this conflict to evolve into a more productive, evidence-based discussion. The ongoing court case on the same issue at the European Court of Justice already provides useful insights into what can actually be disclosed by the agency (see "Additional Information" section below).

As an important aside, CEO also calls MEPs to reject the so-called Trade Secrets Directive, whose final vote in the European Parliament is announced for next April 12. As a matter of fact, one of the numerous problems with this text is that it would give companies additional arguments to fight public interest disclosures in court by threatening public authorities with massive financial penalties would they dare to disclose information they consider a trade secret.

-----------------------------------------------------------------

ADDITIONAL INFORMATION

The European Commission and the pesticides industry fighting Greenpeace Netherlands and Pesticides Action Network Europe at the European Court of Justice on glyphosate documentation

The data used by the European Commission to grant a market authorisation to glyphosate has been a much-debated issue for a long time. Disclosure of industry's dossier has been at the core of a court case started in October 2011 between the European Commission and Greenpeace Netherlands and Pesticides Action Network Europe at the European Court of Justice. The Court's General Court condemned in October 2013 the European Commission to disclose large sections of the documents, but the European Commission has lodged an appeal which is ongoing. From March 2015 onwards, the European Commission has received support from numerous industry groups in this appeal:

- the European Crop Protection Association (‘ECPA’), which argues that “an adequate protection of confidential business information (‘CBI’) is essential in order to preserve and stimulate innovation and thus competitiveness and growth in the EU crop protection sector”;

- CropLife International, the international lobby group of the pesticides industry, whose members “account for approximately 75% of sales across the crop protection industry worldwide” and whose interest consists in “promoting the interests of its members as regards, inter alia, the protection of intellectual property and, in particular, confidential business information”.

- A delegation of US industry, composed of CropLife America, Inc., the National Association of Manufacturers of the United States of America and the American Chemistry Council, Inc., who argue that “the present appeal, since it concerns a conflict between the right of access to documents concerning the environment and the protection of confidential business information that manufacturers of chemical products are required to submit to the competent authority, raises a question of principle which is liable to affect the interests of [their] members”.

- the European Chemical Industry Council, the EU's chemicals industry, arguing that “it has for many years underlined the importance of an adequate protection of confidential business information (‘CBI’) for the competitiveness of the EU chemicals industry.”

- the European Crop Care Association, an association representing small and medium-sized enterprises operating in the generic pesticides industry, who says that “the Court’s judgment in the present appeal will have a significant impact on the small and medium-sized enterprises which it represents, which rely heavily on industrial secrets to protect their intellectual property and innovation.”

Picture: EFSA's headquarters in Parma, Italy, 2012 - by CEO

  • 1. The EU Agriculture and Health Commissioners P. Hogan and V. Andriukaitis, the European Commission's DG SANTE's Director and Vice-Director X. Prats-Monné and L. Miko, the chair of the European Parliament's ENVI Committee G. La Via, Germany's Federal Minister of Food and Agriculture C. Schmidt, etc.
  • 2. They suggested glyphosate could be placed in CLP Category 2, for substances suspected of being carcinogenic to humans.
  • 3. Thanks to the US' Environmental Protection Agency, where the 1983 study is detailed as follows:
    Knezevich, A. and Hogan, G. (1983) A Chronic Feeding Study of Glyphosate (Roundup Technical) in Mice: Project No. 77-2061: BDN-77420. Final rept. (Unpublished study received Aug 17, 1983 under 524-308; prepared by Bio/dynamics, Inc., submitted by Monsanto Co., Washington, DC; CDL:251007-A; 251008; 251009; 251010; 251011; 251012;251013;251014). (MRID 00130406)
    And a 2006 review by the Joint WHO/FAO Meeting on Pesticides Residue where the 1993 study is detailed as follows:
    Atkinson, C., Martin, T., Hudson, P. & Robb, D. (1993a) Glyphosate: 104 week dietary carcinogenicity study in mice. Unpublished report No. 7793, IRI project No. 438618, dated 12 April 1991, from Inveresk Research International, Tranent, Scotland. Submitted to WHO by Cheminova A/S, Lemvig, Denmark.
  • 4. Whose names are also redacted, with more than 80% of them refusing to be identified in a later request by CEO.
  • 5. Interview by CEO, 17 February 2016
In March 2015 the World Health Organisation's International Agency for Research against Cancer (IARC) found the world's most commonly used herbicide, glyphosate, “probably carcinogenic to humans”. Three months later the EU's official risk assessment of the pesticide, conducted by the European Food Safety Authority (EFSA) and Germany's Federal Risk Assessment Institute (BfR), came to the opposite conclusion that glyphosate was “unlikely” to cause cancer to humans. A war of words started with, notably, EFSA's director calling scientists critical of its work (including some involved in IARC's review) “facebook scientists” for a petition they had sent to the European Commission... And it continues with, lately, directors of the two organisations engaging in a public exchange of letters, copied to more or less everyone politically involved on this file,1 where both defended the integrity of their respective institution's work. Eventually, a meeting between the two, meant to take place this week, was cancelled, as EFSA did not agree to the IARC's director's requests to change a number of its statements about IARC's work on its website.One reason behind this almighty mess is the extreme public sensitivity of the topic: behind glyphosate lurks the shadow of US multinational Monsanto, currently one of the most hated companies on the planet, which built its economic development around this wide-spectrum herbicide and GM crops engineered to tolerate it. Monsanto coordinated industry producers into a Glyphosate Task Force (GTF) to facilitate the pesticide's review approval.But the story has more to it than a political tussle. While conflicts are common in science too, resolving them relies on scientists reviewing and debating the evidence. The problem is this step cannot be taken because parts of this evidence are missing. Three industry-sponsored carcinogenicity studies on mice, in particular, are not accessible to IARC while EFSA insists they played an important role in informing its decision. This situation is unfortunately typical of debates on pesticides regulation.This is why for years Corporate Europe Observatory and others have been asking EFSA and the European Commission that, just as with clinical trials for medicines, the data supporting EFSA's scientific opinions should systematically be made public to enable free scientific scrutiny. To find out more about the basis of the glyphosate decision in December 2015 we filed an access to documents request to EFSA to demand the disclosure of these three mouse studies.EFSA refused, and justified this on the basis that the owners of the studies, all industry producers of glyphosate, said disclosing this evidence would undermine trade secrets and intellectual property rights. Corporate Europe Observatory is appealing that decision by EFSA.Meanwhile, the political process goes on, with the European Commission expected (according to EU sources) to propose member states start discussing a new EU-wide renewal of glyphosate's market authorisation next March 7-8. To add to the tension, France's food safety agency ANSES published on 12 February an opinion contradicting EFSA's (even though ANSES officials had contributed to it) by saying that glyphosate could perhaps, after all, be classified2 as a substance suspected of being carcinogenic to humans – a category which would not imply an EU ban – and that more research should be done, in particular by the European Chemicals Agency (ECHA) in Helsinki.The Mysterious ThreeThe starkest difference between the EU's regulatory agencies and the independent scientists who wrote IARC's assessment perhaps lies in their respective interpretation of the animal evidence. The conflict is particularly intense over the EU's use of five industry-sponsored carcinogenicity studies in mice reviewed by BfR and EFSA. Two of these studies, from 1983 (“A chronic feeding study of glyphosate (Roundup technical) in mice 77-2061! (BDN-77-420)”) and 1993 (“Glyphosate: 104-week dietary carcinogenicity study in mice, IRI 438618”), were already included in industry's first EU level request for a market authorisation for glyphosate. But industry sent three new unpublished studies for the EU market authorisation renewal (the “Mysterious Three”, as scientific literature reviews specialist Paul Whaley dubbed them) :- “Carcinogenicity Study with Glyphosate Technical in Swiss Albino Mice” (2001), following OECD Guideline 451 & GLP – study owned by the Israeli pesticides company ADAMA Agan Ltd and was never published;- “Glyphosate technical: Dietary Carcinogenicity Study in the Mouse” (2009), following OECD Guideline 451 & GLP – study owned by the Australian pesticides company Nufarm and was never published;- “HR-001: 18-Month Oral Oncogenicity Study in Mice” (1997), following following OECD Guideline 451 & GLP – study owned by the Japanese pesticides company Arysta LifeSciences Corporation and was never published.The dangerous life of Monsanto employeesThe names of the authors of all five studies are redacted in EFSA's publications. In a Twitter exchange on the matter, Monsanto Europe explained this was for security reasons: “If you get scientists' names what's stopping people going after them/families?” The company later added to its first reply saying: “It's a sad fact that some activists target Monsanto employees for harassment,” but this seems simply irrelevant in this case given that not a single Monsanto employee seems to have been involved in the conduct of these studies.Despite the first two studies, from 1983 and 1993, also not having been published, IARC could access3 them. Indeed it interpreted the 1983 study as showing “a significant increase in the incidence of rare tumours, with a dose-related trend, which could be attributed to glyphosate”, in stark contrast with EFSA and BfR's review of the same study. IARC's interpretation of the 1993 study is on the other hand consistent with EFSA and BfR's. But it could not evaluate the three more recent studies, even though it was able to access summaries which its scientists commented showed incidence of various tumours.“Key” and “pivotal” evidenceThe Mysterious Three are an essential element of the conflict. This is particularly so because EFSA heavily referred to them to explain its assessment, with José Tarazona, the Head of EFSA's Pesticides Unit in charge of the assessment, calling them “key” and “pivotal”. Similar comments can be found from various member states' experts,4 with Belgium insisting that “it was unfortunate that IARC did not take into account 3 guideline studies in both mice and rats, since this could have put the overall conclusions in another perspective”. This very unfair sentiment (IARC could not access these studies) was echoed by Ireland: “IARC's failure to evaluate the 3 other studies is not helpful.”Since EFSA's publication, the agency has been arguing that there is enough detailed information in its documentation to perform a good analysis, but IARC scientists respond that the descriptions and summaries published miss key elements and cannot replace original data. Among these missing elements, IARC said,5 are "the historical control data from the reporting laboratory for all tumours with statistically significant positive increases, by either test recommended by OECD; another is the survival of the animals". More generally, IARC pointed to its list of attention points for all studies it assesses. [18 February 2016 addition]Secret perfection or convenient argument?So what is in these Mysterious Three? How can only three studies explain such a striking contrast? Would they be so strong as to convince IARC to reverse its stance? Would they on the contrary confirm it? Or, given the strong political interest in this file and the fact that the EU's Pesticides Regulation would force glyphosate out of the market were its cancer-causing properties confirmed, isn't referring to these secret studies a convenient argument for all those willing to keep glyphosate on the EU market anyway?In its response to Corporate Europe Observatory on 5 February 2015 explaining why it would not release the information, EFSA said that the studies' owners (who, by law, must be consulted) refused any disclosure because they considered their studies to contain trade secrets and intellectual property which if released would harm their industrial and commercial interests as well as their “competitive position”. EFSA agreed with this analysis and explained that, according to the exception foreseen in the EU's Public Access to Documents Regulation 1049/2001 as well as in the EU's Pesticides Regulation 1107/2009, it was entitled to not disclose the documents.Abusive use of the trade secrets protection argumentHowever, both regulations only protect commercial interests and, in the case of the Pesticides Regulation, a limited list of elements within the studies, not the whole document – it is difficult to believe that everything in a scientific study would be a trade secret. Moreover, the EU's Pesticides Regulation stipulates that any data owner refusing disclosure of its material must provide a verifiable proof that disclosure would harm him, which was apparently not done. Finally, glyphosate has been off-patent for 15 years and most pesticide companies now producing glyphosate belong to the Monsanto-led Glyphosate Task Force, the group that bundled all these studies together and sent them to the BfR and EFSA: how would disclosing these studies harm any of these companies' competitive position if they were already shared among the main competitors?As a consequence, CEO is appealing this decision, hoping that EFSA will use the opportunity of this major file and controversy to demonstrate its good faith in actually acting upon its declared intentions on data transparency and providing a level of openness that enables this conflict to evolve into a more productive, evidence-based discussion. The ongoing court case on the same issue at the European Court of Justice already provides useful insights into what can actually be disclosed by the agency (see "Additional Information" section below).As an important aside, CEO also calls MEPs to reject the so-called Trade Secrets Directive, whose final vote in the European Parliament is announced for next April 12. As a matter of fact, one of the numerous problems with this text is that it would give companies additional arguments to fight public interest disclosures in court by threatening public authorities with massive financial penalties would they dare to disclose information they consider a trade secret.-----------------------------------------------------------------ADDITIONAL INFORMATIONThe European Commission and the pesticides industry fighting Greenpeace Netherlands and Pesticides Action Network Europe at the European Court of Justice on glyphosate documentationThe data used by the European Commission to grant a market authorisation to glyphosate has been a much-debated issue for a long time. Disclosure of industry's dossier has been at the core of a court case started in October 2011 between the European Commission and Greenpeace Netherlands and Pesticides Action Network Europe at the European Court of Justice. The Court's General Court condemned in October 2013 the European Commission to disclose large sections of the documents, but the European Commission has lodged an appeal which is ongoing. From March 2015 onwards, the European Commission has received support from numerous industry groups in this appeal:- the European Crop Protection Association (‘ECPA’), which argues that “an adequate protection of confidential business information (‘CBI’) is essential in order to preserve and stimulate innovation and thus competitiveness and growth in the EU crop protection sector”;- CropLife International, the international lobby group of the pesticides industry, whose members “account for approximately 75% of sales across the crop protection industry worldwide” and whose interest consists in “promoting the interests of its members as regards, inter alia, the protection of intellectual property and, in particular, confidential business information”.- A delegation of US industry, composed of CropLife America, Inc., the National Association of Manufacturers of the United States of America and the American Chemistry Council, Inc., who argue that “the present appeal, since it concerns a conflict between the right of access to documents concerning the environment and the protection of confidential business information that manufacturers of chemical products are required to submit to the competent authority, raises a question of principle which is liable to affect the interests of [their] members”.- the European Chemical Industry Council, the EU's chemicals industry, arguing that “it has for many years underlined the importance of an adequate protection of confidential business information (‘CBI’) for the competitiveness of the EU chemicals industry.”- the European Crop Care Association, an association representing small and medium-sized enterprises operating in the generic pesticides industry, who says that “the Court’s judgment in the present appeal will have a significant impact on the small and medium-sized enterprises which it represents, which rely heavily on industrial secrets to protect their intellectual property and innovation.”Picture: EFSA's headquarters in Parma, Italy, 2012 - by CEO 1. The EU Agriculture and Health Commissioners P. Hogan and V. Andriukaitis, the European Commission's DG SANTE's Director and Vice-Director X. Prats-Monné and L. Miko, the chair of the European Parliament's ENVI Committee G. La Via, Germany's Federal Minister of Food and Agriculture C. Schmidt, etc. 2. They suggested glyphosate could be placed in CLP Category 2, for substances suspected of being carcinogenic to humans. 3. Thanks to the US' Environmental Protection Agency, where the 1983 study is detailed as follows:Knezevich, A. and Hogan, G. (1983) A Chronic Feeding Study of Glyphosate (Roundup Technical) in Mice: Project No. 77-2061: BDN-77420. Final rept. (Unpublished study received Aug 17, 1983 under 524-308; prepared by Bio/dynamics, Inc., submitted by Monsanto Co., Washington, DC; CDL:251007-A; 251008; 251009; 251010; 251011; 251012;251013;251014). (MRID 00130406)And a 2006 review by the Joint WHO/FAO Meeting on Pesticides Residue where the 1993 study is detailed as follows:Atkinson, C., Martin, T., Hudson, P. & Robb, D. (1993a) Glyphosate: 104 week dietary carcinogenicity study in mice. Unpublished report No. 7793, IRI project No. 438618, dated 12 April 1991, from Inveresk Research International, Tranent, Scotland. Submitted to WHO by Cheminova A/S, Lemvig, Denmark. 4. Whose names are also redacted, with more than 80% of them refusing to be identified in a later request by CEO. 5. Interview by CEO, 17 February 2016
 

Comments

Submitted by Christine T. (not verified) on

Dr. A. Samsel and S. Seneff just recently published an article with Monsanto's glyphosate safety data from 80's (available to them through the FOIA), showing that already at that time the carcinogenicity of that compound was known.
The journal Journal of Biological Physics and Chemistry 15 (2015) devoted the entire volume to glyphosate's catastrophe, including the Samsel+Seneff article, available at:
http://responsibletechnology.org/irtnew/wp-content/uploads/2015/11/Glyph...
Title of their study:
"Glyphosate, pathways to modern diseases IV: cancer and related pathologies"
Similar conclusions of that study are reflected in another article of that issue, written by Dr. M. Cuhra, all available at:
http://www.amsi.ge/jbpc/31515/jbpc31515.html
Both articles were written after inspection of the until last Sep 'secret original glyphosate studies'.
There is another 16-pages long article in that volume 13, very much worth reading:
"The sixth mass extinction and chemicals in the environment: our environmental deficit is now beyond nature’s ability to regenerate" starting on p.160.

Submitted by Nancy Swanson (not verified) on

The names are blacked out in the BfR Toxicology report, but the numbers are not. They can be traced in the appendix: Glyphosate_RAR_40_list of studies_version 1_CA-CP_2013-12-18.pdf

Here are your authors:
Knezevich, A. L.; Hogan, G. K.
1983 A chronic feeding study of glyphosate (Roundup technical) in mice
77-2061 ! (BDN-77-420)
TOX9552381

Kumar, D.P.S.
2001 Carcinogenicity Study with Glyphosate Technical in Swiss Albino Mice
TOXI: 1559.CARCI-M FSG
GLP: Y, published: N
2309396 / ASB2012-11491
Owner: FSG (Feinchemie Schwebda GmbH)

Wood, E., Dunster, J., Watson, P., Brooks, P.
2009 Glyphosate Technical: Dietary carcinogenicity study in the mouse
SPL 2060-0011 NUF
GLP: Y, published: N
2309412 / ASB2012-11492
Owner: NUF (Nufarm GmbH & Co. KG)

Sugimoto, K.
1997 HR-001: 18-Month Oral Oncogenicity Study in Mice
IET 940151 ALS
GLP: Y, published: N
2309415 / ASB2012-11493
Owner: ALS (Alschu-Chemie GmbH)

Atkinson, C., Strutt, A.V., Henderson, W., Fich, J., Hudson, P.
1993 Glyphosate - 104 week combined chronic feeding / oncogenicity study in rats with 52
week interim kill (results after 104 weeks)
7867 CHE
GLP: Y, published: N
2309374 / TOX9750499
Owner: CHE (Cheminova A/S)

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The official EU assessment of glyphosate was based on unpublished studies owned by industry. Seven months later, the pesticide industry still fights disclosure and, so far, successfully. We obtained a copy of their arguments.

The European Commission proposal on scientific criteria defining endocrine disruptors (EDCs) is the latest dangerous outgrowth of a highly toxic debate. The chemical lobby, supported by certain Commission factions (notably DG SANTE and the Secretary-General) and some member states (UK and Germany), has put significant obstacles in the way of effective public health and environment regulation.

This May is dense on the EU chemicals regulation front. Crunch time for two major files: the European Commission needs to publish the identification criteria for endocrine disrupting chemicals, and together with EU States must decide how, or not, renew the market approval of glyphosate, an herbicide produced and defended by Monsanto. Last week, the Professor Alan Boobis happened to be involved in both.

Demonstrating the problematic symbiosis between corporate interests and EU institutions, the same lobbying consultancies often get hired by both.

The official EU assessment of glyphosate was based on unpublished studies owned by industry. Seven months later, the pesticide industry still fights disclosure and, so far, successfully. We obtained a copy of their arguments.

While CEO is not taking a position on the UK referendum, many of our publications are relevant to those who will have a vote, or those who are following the debate.

Biodiversity collapse, the future of agriculture, politics versus science, EU States and the European Commission shifting blame on each other, industry's capture of the regulatory process through data secrecy, a Commissioner caught between Juncker, EU States, lobby groups, and his own services... The glyphosate saga, coming to the end of its first phase tomorrow, has been an entry point into many broader problems. Overview.

The European Commission proposal on scientific criteria defining endocrine disruptors (EDCs) is the latest dangerous outgrowth of a highly toxic debate. The chemical lobby, supported by certain Commission factions (notably DG SANTE and the Secretary-General) and some member states (UK and Germany), has put significant obstacles in the way of effective public health and environment regulation.

The corporate lobby tour