Kovidh Pharma is just with highest expertise in the domain, our splendid team has been serving businesses and researchers around the globe since long time.
We as a knowledge based partner for Pharma and biotech companies, independently caters all support in clinical and pre clinical research. It is a leading service provider based in Hyderabad, India.
The strong compliance knowledge, global understanding is a key success to any organisation which is our strength. We take care of your GCP, GLP and applicable regulatory requirements. The comprehensive services range from clinical trials phase I - IV, Bioavailability/Bioequivalence & pre clinical studies etc.
Our Services
To achieve the highest standards of professional excellence by conducting our duties in highly ethical environment and providing our services with honesty, quality and compliance to our clients, stake holders.
To be a preferred and globally respected research partner for Pharmaceutical and Biotech, medical devices and healthcare companies.
We strongly believe in Trust and Transparency, Integrity and Reliability, Speed and Timely Delivery, Best Quality and Total Compliance, Team work and Commitment, Innovative on and Creativity.
With over 25 years of expertise, our leader is a distinguished authority in clinical research and pharmaceutical industries. Widely recognized for his exceptional knowledge and experience, he brings unparalleled insight and guidance to our organization.
Dr. Ravi Kanneti is the Founder & Director of Kovidh Pharma, where he is responsible for organizing and implementing operational strategies for the entire company. With over 25 years of professional experience in clinical research and pharmaceutical companies, Dr. Kanneti brings a wealth of knowledge and expertise to his role.
Throughout his career, Dr. Kanneti has been associated with prominent organizations such as Lupin Pharmaceutical Ltd, Dr. Reddy's Laboratories Ltd, Actimus Bioscience Pvt. Ltd, Synchron Research Services Pvt. Ltd, Micro Labs Ltd, and Johnson and Smith Pharmaceuticals Ltd., where he has headed various portfolios.
He completed his PhD in Pharmacy (Pharmacology) from LMCP, GU, India, and a Master of Pharmacy in Clinical Pharmacy/Pharmacy Practice from UDP, AU, India.
Dr. Kanneti's professional experience spans GCP, GLP, GXP, and applicable regulatory requirements for conducting various bio studies, including PK/PD, BA/BE, CT, PV, in-vivo & in-vitro, as well as clinical and preclinical studies. He has extensive experience with different dosage forms such as tablets, capsules, inhalations/nasal preparations, biosimilars, and dermal products. His expertise also includes QMS and CR projects PM/DM for various therapeutic groups in support of drug development processes for IND, NDA, ANDA, and 505(b)2 submission studies.
He has a proven track record in designing and implementing quality systems at reputed CROs and Pharma R&D setups. Dr. Kanneti is experienced in maintaining data integrity and compliance at both site and corporate levels and has successfully handled various regulatory audits and inspections, including those by the FDA, WHO, ANVISA, EMEA/MHRA, AFFSAPS, TGA, NABL, and CDSCO.
Years expertise, he is widely acknowledged as an expert in clinical research and pharma companies.
Our commitment to quality, integrity, and compliance ensures that we deliver exceptional results that meet the highest industry standards. Whether you are looking for expert guidance on clinical trials, regulatory affairs, data management, or audit readiness, we are here to help. Reach out to us today to discuss how we can partner together to accelerate your research and bring your pharmaceutical innovations to market with confidence.