PharmaVigil is a global Consulting & outsourcing company incorporated in India in 2019, offering advisory and outsourced support to the pharmaceutical industry and regulatory authorities. PharmaVigil is backed by 50 years of collective intelligence of its founding groups and works with leading marketing authorization holders and pharmaceutical companies globally.
PharmaVigil is closely associated with various regulatory authorities to be able to support companies and authorities with some updated and comprehensive solutionsPharmaVigil has some of the most highly experienced professionals to serve our diverse client base and helping them in meeting their objectives, compliance, and patient outcomes.
We support our clients with a complete set of Pharmacovigilance obligations compliance services. Whether that means helping clients establish their own global quality PV system, upgrading their existing systems or ensuring recurring activities.
PharmaVigil team prepares complete life-cycle of a regulatory dossier, supporting all the major steps in the preparation of a submission, liaison with the regulators for and on-behalf of our clients.
We develop clinical study/BA-BE study protocols, clinical study reports, clinical patient safety narratives, investigator brochures, Informed consent forms, Clinical Overview (CO), Non-Clinical Overview (NCO), AtCO and other documents.
OOur team is qualified and experienced in toxicological risk assessment, provide comprehensive services to meet your GMP needs and has helped products pass the rigorous regulatory scrutiny and reach the market.
With current legislation application, it is mandatory for MAHs/applicants to establish their own PV quality system to take care of their products safety. Our experts render support in establishing/upgrade PV system PV system in-line with the applicable regulatory authority recommendations.
PharmaVigil delivers global solutions by empowering subject matter experts from across the world. Our network offer the global reach and local depth to navigate regulatory challenges around the world. The team is in close contact with the local authorities and as a group we are well versed with the applicable updated regulations.
The applicant company’s products must demonstrate quality, efficacy and safety to get the Marketing Authorization by a Regulatory Agency. This is of utmost importance in a complete product life-cycle. Our experts take care of end to end product cycle support to the MAHs/applicants.
is serving global pharmaceutical industry since 2009 for regulatory and legal services. Meher Pharma International is bestowed with many national and international awards for its valuable contribution to the pharmaceutical industry.
The group has extended its service portfolio majorly into pharmacovigilance and scientific and medical writing services.
The group is associated with global regulatory consultants and this relation helps in registering products and manufacturing unit of our clients across the globe on fast track. The group guides you to launch your own export division.
The team has proven ability to advise and manage a variety of projects of all sizes.