Healthcare.
Regulatory Services and Registration
Prakhar provides services in Drug Regulatory Affairs. Our regulatory experts compile the dossiers (DMF, ASMF, APIMF, Dossier), publish in eCTD format through software and facilitate to file in regulatory agencies. Experts help the companies in addressing the deficiencies of regulatory agencies if requested during review of application.
Third Party Manufacturing
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Audit and Traning
GMP Compliance | GMP Consultancy Services | GMP Audit Pharmaceutical | GMP Gap Analysis Audit | GMP Training | DMF/Dossier Preparation | cGMP Consulting Services | Quality Management Systems | Technical Document Writing
Prakhar has qualified auditors perform third party audits of manufacturers of Drug Products, Active Pharmaceutical Ingredients, Raw Materials, Packing Materials and Intermediates.
Pharmacovigilance
We associated with trusted Medical team to write PSUR RMP PSMF support with full query response.
Export Marketing and Consultancy
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ELTD Publication and Reports
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Yoga and Certification
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In 2020, we made new long-term commitments to sustainable development.
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