Meher Pharma International is a pharmaceutical regulatory and legal advisory. Since inception in 2009, we have gained confidence of our customer by rendering customised services on time. Our expertise and experience team focus on achieving full commercial potential for all products. Our team has proven ability to advise and manage a variety of projects of all sizes. We have list of satisfied clients from across the world.
We have extended our service portfolio majorly into pharmacovigilance and pharma legal services. We have also introduced diploma courses and relevant publishing for pharmaceutical industry aspirants.
We are associated with global regulatory consultants and this relation helps in registering products and manufacturing unit of our clients across the globe. We are capable to assist and advise to launch your own export division.
We are advising clients to register new drug, medical device, bulk drug, cosmetics etc in India. This is a good platform for the companies who are willing to enter into export.
We advise on following legal services to pharmaceutical companies. Drug Criminal Cases, Drug Prosecution, Trade Mark and Patent Dispute, NPPA Litigation, Public Interest Litigation, etc.
Book is like a teacher, like a mentor that positively impact on readers thinking behaviour and attitude. Practical book is always better than a theoretical book.
Industry is always facing shortage of trained work force or talented work force. When you appear for interview you won’t feel confident because you know only theory and not practical.
Human resource consulting approach allows us to advise on all aspects of people management, helping our clients to create value for their people – or face losing their most valuable assets.
Medical Writing is a proven tool to educate doctors and healthcare associate for brand image, brand recall and brand retention. We have hand on experience of writing.
National Pharmaceutical Pricing Authority (NPPA) is an organization of the Government of India to fix/revise the prices of controlled bulk drugs and formulations.
We are assisting clients in legalising documents from embassies after legalisation from chamber of commerce and ministry of external affairs. We have loyal clients from Gujarat, Maharashtra, etc.
FSSAI has been created for laying down science based standards for articles of food and to regulate their manufacture, storage, distribution, sale and import to ensure availability of safe...
Medicine is a double edged sword either saves life or kills life. It all depends how you care medicine from manufacturing till distribution points. How do you store and how clinicians give feedback.
We advise on getting method analytical method validation of Assay, impurities and of residual solvents, process validation (PV), related substance analysis. dissolution profile.
We advise on filing applications for following services : Import Registration of Cosmetics, Import Registration of Drugs/API, Import Registration of Medical Device, Import Registration of Biological.
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