Biosynergetics, Inc. provides independent biomedical and medical research and consulting resource specializing in Biomedical Engineering and Pharmaceutical Science. Biosynergetics, Inc. has extensive experience in the pharmaceutical industry, including clinical trial design and monitoring, the evaluation of drug delivery, toxicity, and adverse drug events.

Biosynergetics, Inc. also owns various intellectual property rights developed internally involving concentration modification of compounds in flowing fluid systems, and energy collection devices.

Areas of Expertise:

• Biopharmaceutics, Pharmaceutical Science and Biomedical Engineering
• Extensive Experience for all Manner of Compound Investigation
• Clinical Pharmacology, Pharmacokinetics, Pharmacodynamics
• Absorption, Distribution, Metabolism, Elimination
• Drug Regimen Design, Dosage-Form Design and Drug Delivery
• Drug Interactions, Side Effects, Toxicity, Adverse Events and Injury
• Clinical Trials and Large Scale Population Analysis
• Mathematical Modeling
• Industrial Pharmaceutics and Manufacturing Processes
• Scientific Document Preparation, Regulatory Submission Analysis and Review
• In-Vitro/In-Vivo Data Correlation, Animal Data Studies and Scale-Up
• Company Acquisitions and Biotechnology Contract Research

The CECON Group, Inc.

Consulting in Chemistry, Chemical Engineering, Materials, Nanotechnology, Mechanical Engineering, Pharmaceuticals, Biotechnology and Related Science and Engineering Fields. Technical Experts with Experience in Patent Litigation, Products Liability and Personal Injury.

Our inside technical professionals will help you find the expert you need, either from CECON's network of over 1000 science, engineering, and technical business experts, or by doing a custom search. We will help you find the best consultant for your project. Advantages are:

As Dodds & Associates, Dr. David Dodds provides experience in the Pharmaceutical, Biotech, and Chemical Industries across multiple disciplines; organic synthesis, chiral chemistry, biocatalysis, molecular biology, industrial biotech, fermentation of natural products (anticancer and antibiotics) and recombinant enzymes, plus the associated downstream processing, all within the GMP regulatory environment. This experience is generally in process development and CMC (Chemistry, Manufacturing, and Control) sections of IND and NDA filings with the FDA.

Relevant experience includes IP review and strategy, expert witness for patent defense (depositions, affidavits and cross-examination), technical support of patent prosecution, technical due diligence, and service on technical advisory boards.

Dr. James C. Norris, Ph.D., DABT, EURT is an Expert Witness in Toxicology and Pharmacology. He has Litigation and Arbitration experience in the United States, United Kingdom and Hong Kong. Dr. Norris has given testimony to government agencies, has acted as a consultant for the media (BBC) and is an Industrial Site Crisis Team Member. He is avaliable for both Plaintiff and Defense.

Areas Of Expertise:

45+ years of independent, multi-disciplinary scientific experience in basic and applied research, university teaching and large commercial laboratory operations for your litigation/consultation needs. Nationally known expert in over 400 individual, consolidated and class action cases. Daubert - qualified.