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Email: rlphelps@usa.net

 

 

 

 

 

 

 

President and Principal Advisor

Robyn L. Phelps, MSc, PhD is a Toxicologist and Safety Pharmacologist with 25 years of scientific and drug development experience.  She has expertise in nonclinical pharmaceutical research and development, and has specialized skills in animal model development, cardiovascular and pulmonary safety pharmacology.  Dr. Phelps has experience in all routes of administration including dermal and inhalation.  Her study experience includes acute, subchronic and chronic toxicity,  carcinogenicity and reproductive toxicology in multiple species.  Dr. Phelps is an experienced manager who can provide both high level and study specific oversight.  She is knowledgeable of domestic and international regulations and routinely interacts  with regulatory authorities.   She has authored nonclinical documents for national and international submissions as well as scientific manuscripts.  Dr. Phelps serves as a corporate scientific advisor and is a member of the Roundtable of Toxicology Consultants.

For details, click the icon to view Dr. Phelps's CV: 

Principal Advisor

Jan Bernal,  BSc, DVM, is a Veterinarian with 14 years of experience in veterinary medicine and surgery, nonclinical research, and drug development. Dr. Bernal has held positions in both clinical veterinary practice and nonclinical contract research organizations.  Her expertise includes small animal, laboratory animal, and primate medicine as well as animal colony management and regulatory adherence. She is a surgical expert skilled in the development and utilization of unique models of drug administration and monitoring technologies, and is an experienced study director.  Dr. Bernal served on the Board of Directors for the Academy of Surgical Research and has published articles on telemetric monitoring and infusion device and delivery models.

For details, click the icon to view Dr. Bernal's CV: 

Principal Pathologist

Dan H. Lochner,  DVM, MSc, Diplomate ACVP,  is a Veterinary Pathologist with more than 22 years experience in toxicologic pathology, drug safety and chemical toxicity.  He has held appointments in academics and in drug development both in the USA and Switzerland, and is conversationally fluent in German.  Dr. Lochner's range of experience includes the pathologic/histopathologic assessment of acute, subchronic and chronic toxicity,  carcinogenicity and reproductive toxicology studies in multiple species, including non-human primates.  He has experience in all routes of administration including dermal and ocular application/implantation, and inhalation.  Dr. Lochner is an experienced author of toxicology/pathology reviews for national and international regulatory submissions.

For details, click the icon to view Dr. Lochner's CV: 

Biomedical Engineer

John R. Decker, BSE, Electrical Engineering, Graduate Studies, Physiology, has extensive experience in Inhalation Technology including instrument and software development, and biologic testing.  Mr. Decker is a well-recognized leader in the inhalation field who has dedicated a 40 year career to understanding the biological effects of environmental conditions on animals.  His background includes generation and monitoring of inhaled pharmaceuticals, radionuclides, vapors and gases, smoke and chemical aerosols.  He is an experienced program manager who has developed, constructed, installed and validated numerous regulatory-compliant automated systems for whole-body and nose-only inhalation exposure systems used by the National Toxicology Program, government, chemical industry, and pharmaceutical clients.  In addition to the provision of program-specific engineering and monitoring services, Mr. Decker is an excellent staff trainer.

For details, click the icon to view Mr. Decker's CV: 

 

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Last modified: 05/09/08