© Joint Commission Resources TJC – POCT In Toto Meeting Joint Commission standards in the POC Laboratory Judy Gabriel, MT(ASCP) BS, MA Field Representative.
23andMe and FDA A Legal Perspective. Outline 1.FDA Background - Zach 2.About 23andme - Laura 3.FDA letter and arguments - Zach 4.23andme potential defenses.
2011 Food Defense Summit: Legal Risks and Responsibilities for Producing Safe Food
The Documented Health Risks of Genetically Engineered Foods (Long Version)
Dr. Richard Raymond - Antibiotics used in animals Raised for Food - Perception vs. reality
1 Petition to Convert Claritin®, Allegra® and Zyrtec® to OTC Status Robert Seidman, PharmD, MPH Chief Pharmacy Officer WellPoint Health Networks FDA Pulmonary.
Jan Zolkower, MSHL, CIP, CCRP January 13, 2012. Review Investigator Responsibilities Discuss recent FDA Warning letters and OHRP Determination letters.
1 Liability and Risk William D. Marler, Esq. [email protected].
Medicare Submission for Pre-Approval in Clinical Research Ronda Sharp, R.N., B.S.N., C.C.R.C. Clinical Research Facilitator Methodist Research Institute.
Foodborne Illness CSI: Milwaukee North Shore Rotary Club October 23, 2006 Cracking the Legal Code.
Example of Adulterated and Misbranded Drugs
Investigator Responsibilities for Research
