Pre-Clinical and Clinical Research
for Drug Product Development
Preclinical Research Services:
Hayat Pharmaceutical Consultants (HPC) offers specialized preclinical research services. Our expertise spans a wide range of in vivo non-GLP and GLP safety assessment solutions in both rodent and non-rodent species to thoroughly evaluate pharmaceuticals, biologics, animal health products, agrochemicals, and biocides. Our scientific and regulatory teams develop customized research programs and conduct individualized preclinical studies to ensure that your IND/NDA-enabling toxicology, safety pharmacology, and laboratory studies comply with global regulations.
Clinical Research Services for Early Phase Drug Development:
At, Hayat Pharmaceutical Consultants we understand that each drug development project is unique and deserves the most efficient, high quality clinical research services, to advance through the early phases of drug development quickly and seamlessly.
Advancing your drug candidate smoothly to proof of concept is what we do best. Work with clinical research services experts who leverage your preclinical data in the design and conduct of critical early phase research and generate high-quality data to inform the best decisions for your program. Whatever the size of your biopharmaceutical company, you can benefit from our expertise in the clinical pharmacology studies required for regulatory submissions, in a wide range of therapeutic areas, for small molecules and biologics, within NDA or Hybrid applications.
HPC, through its partnership with Trial360 conducts pre-clinical and clinical trials for the sponsors around the globe in a cost and time effective manner. Our organization is comprised of highly qualified staff, well versed in conducting animal studies.
We have validated animal models to screen NCEs or formulations to evaluate their safety and efficacy. Stock of laboratory animals include Rabbits, Mouse, Rats, Guinea pigs, Hamsters, Dogs etc. A dedicated team will be assigned to your project to work tirelessly from drafting a protocol through execution and finalizing the report in close collaboration with sponsors. Our lab will be just an extension of yours and you will have full visibility of the progress and operations through Phase I to Phase IV clinical trials, we can also adopt to your project at any stage of the development and progress through to completion from there.
