J.V.A.G. Pharma Consultants

J.V.A.G. Pharma Consultants is rated 3 out of 5 in the category pharmaceuticals. Read and write reviews about J.V.A.G. Pharma Consultants. We are one of the leading and reliable Regulatory Consultants across the Globe. We are specialized company with an Experienced, Multitasking, Capable & Confident team for taking up the complete Regulatory Project responsibility to offer you high speed quality services. Our team has the core values of Integrity, Discipline, Teamwork, Commitment and Ethics; we wish to offer these services with an aim to explore an alliance between our partner and us that could help to break new ground in sales and marketing. Our Regulatory Services are tailored to meet client’s requirements and add value to their organization by minimizing both Time and Money spent We extend our services with the following aspects of Pharma Regulatory Affairs :- 1. DMF (Preparation, Filling and Registration of Drug Master Files for API. Type II, III, IV for API, Primary Packaging Materials and Excipients respectively). 2. Scale up and Tech. Transfer Projects for Finished Formulations; various Dosage Forms. 3. Dossiers services (Documentation of CTD’s, ACTD’s, eCTD’s etc... of Finished Formulations e.g. Tablets, Capsules, Injections, MDI’s, DPI’s, Nebulisers, Gels, Ointments and many more). 4. Guidance for GMP, GCP, GLP and updation of same. 5. Post submission query reply, Query solving & Experts opinion on same. 6. BA/BE Studies. J.V.A.G. provides Best Approved and EU/US agency audited CRO’s for performing all the mentioned studies 7. Phase II, III, IV Clinical trials & Toxicity studies 8. Preparation of SPC’s, Package information leaflets (PIL), Periodic Safety Update Reports (PSUR’s). 9. COS/CEP Preparation / Submissions & Audits. 10. The Experienced panels of experts can advice you on strategic, cost effective and innovative product development planning’s, system setups for cGMP according to WHO / USFDA / MHRA / MCC / ICH guidelines as well as GMP Compliance, starting right from Plant Design to GMP Approval by any Regulatory Agency worldwide. 11. We also have organization based Regulatory Training Programs for the Students and the Regulatory Professionals. 12. Provide liasoning services in India for Importers and Exporters,Legal Services. We have a team of 24 Pharmacists well Trained and Experienced in Regulatory preparation and submission so we can surely speed up your dossier compilation there by submission and there by Marketing of the products. We have proven track of offering these dossiers successfully in Tunisia /Algeria / Morocco / Egypt / Turkey / Poland / Romania / Vietnam / Mexico /Malaysia / Indonesia / Chile / Jordan / etc. We also offer CDs, for Technologies for Tablets / Capsules / Ointment / Eye Drops / Injetables / MDI / Nasal Sprays and Drops / Specialty Tabs like DR, EC, MDT, etc. Please inquire with us regarding the same ([email protected]) Please visit our website (www.jvagpharma.com) for further details.