PharmaLeaf is an independent consultancy providing customized technical and regulatory support to several Global and Indian companies, Contract Research Organizations, Laboratories, Logistics etc., i.e. any stakeholder involved with drug research, product development, clinical trials, testing, manufacturing and supplies. PharmaLeaf’s expertise lies in “building consensus” on regulatory challenges to successfully navigate approvals for complex projects. All underlying issues are addressed from our technical knowledge domain by subject experts, supported by hands on experience and negotiation skills. These are benchmarked, across markets, for best regulatory practices, so that we can offer our client the most efficient solution. PharmaLeaf provides Regulatory support to projects with New Chemical Entities, Generic Drugs, Controlled Drugs (narcotics & psychotropics), Biotechnology Products & Vaccines, Biologicals & Blood Products, Medical Devices & Diagnostics, Over the Counter Drugs, Herbals & Nutraceuticals, Cosmetics & Body Care Products etc. We provide Technical and Regulatory support to projects within 3 service verticals i.e. Clinical Trials, Marketing Authorizations and Audits.