Gad Consulting Services is a nine year old toxicology and regulatory consulting firm which offers services in biocompatibility testing for all aspects of drug development. We offer clinical and biocompatibility testing in order to more quickly yield marketable healthcare solutions. Each and every project is considered and tended to individually and independently, but with the benefit of more than 25 years experience in the field and regular ongoing interactions with FDA. We are a small organization priding ourselves on offering timely, quality, and cost effective services in the area of biocompatibility testing to ensure safety and compliance with FDA requirements.
Gad Consulting Services is a nine year old consulting firm which offers services in occupational toxicology. We have successfully served the needs of more than 150 client firms in the fields of pharmaceutical development and regulation, biotechnology, medical device development and registration, litigation support and expert witness services, experimental design, statistical analysis and risk assessment, dietary supplement evaluation and review, occupational toxicology, and training. Dr. Gad initiated and managed the occupational toxicology program at Searle, identifying needs, developing data and generating Material Safety Data Sheets for all compounds and process intermediates, making them available worldwide by an electronic system.
Gad Consulting Services is a nine year old toxicology and regulatory consulting firm which offers services in clinical and biostatistics report writing for all aspects of drug development. We offer clinical and biostatistics report writing in order to more quickly yield marketable healthcare solutions. Each and every project is considered and tended to individually and independently, but with the benefit of more than 25 years experience in the field and regular ongoing interactions with FDA. We are a small organization priding ourselves on offering timely, quality, and cost effective services in the area clinical and biostatistics report writing.
Gad Consulting Services is a nine year old toxicology and regulatory consulting firm which offers services in clinical data management for all aspects of drug development. We offer clinical data management strategies in order to more quickly yield marketable healthcare solutions. Each and every project is considered and tended to individually and independently, but with the benefit of more than 25 years experience in the field and regular ongoing interactions with FDA. We are a small organization priding ourselves on offering timely, quality, and cost effective services in the area clinical data management.
Gad Consulting Services is a nine year old toxicology and regulatory consulting firm which offers services in medical device development. Medical device and diagnostic development services include program design, monitoring, report preparation/review, clinical safety studies, expert reports, position papers, and more. Each and every project is considered and tended to individually and independently, but with the benefit of more than 25 years experience in the field and regular ongoing interactions with FDA. We are a small organization priding ourselves on offering timely, quality, and cost effective services in the area of medical device development.
Gad Consulting Services is a nine year old toxicology and regulatory consulting firm which offers services in Drug development. We have successfully served the needs of more than 150 client firms in the fields of pharmaceutical development and regulation, biotechnology, medical device development and registration, litigation support and expert witness services, experimental design, statistical analysis and risk assessment, dietary supplement evaluation and review, occupational toxicology, and training. We are a small organization priding ourselves on offering timely, quality, and cost effective services in the drug development area.
Gad Consulting Services is a nine year old toxicology and regulatory consulting firm which offers services tailored to meet the needs of its clients in the areas of the Principals expertise. We have successfully served the needs of more than 150 client firms in the fields of pharmaceutical development and regulation, biotechnology, medical device development and registration, litigation support and expert witness services, experimental design, statistical analysis and risk assessment, dietary supplement evaluation and review, occupational toxicology, and training. We are a small organization priding ourselves on offering timely, quality, and cost effective services in the toxicology area.