Tech-Doc-Solution Consultancy -Api/Pharma/Cro/ Educational Institute Email & Phone Number

*Audit, Training and Consulting - GMP Compliance for pharma bulk drugs and allied Industries. Our mission is “Simplify GMP for Humanity.” * GMP Vendor Audit, international buyer get fair assessment of GMP standards of KSM, API & Excipient Manufacturers across the world.* We are here to help you with any vendor qualification audit with reference to ICH Q7, PICS, EU GMP, EUDRA, or any other guidelines as required by you, We have a set up to conduct online as well as on- site audits that suit your requirements. * Formulation plant gap assessment audit(Regulatory/ Accreditations such as ISO/ GMP)* Project management.* We have written, compiled and filed more than 120 registration dossiers to CIS, GCC, SFDA, PMDA, LATAM, Korea, ASEAN and other RoW markets across the globe. Filings in different formats like eCTD/ACTD/NeeS/CTD also we do assist in query solving.* Technical assistance in Microbiological techniques and procedures.* Computer system validation service.* Trainings for technical and regulatory upgradation.* Clinical research - BA/BE Studies* QMS/ Technical/ Audit compliance purpose Documentation.* Validation and Compliance activities and setting up of New departments with Engineering layouts,