31 YEARS
Since 1994
Products / CMO / CDMO

Custom Synthesis & Contract Manufacturing

Services

Custom Synthesis & Contract Manufacturing

VPCL offers long-term Contract Manufacturing Services right from strategic partnerships in development, validations, DMF filing and commercial manufacturing of Active Pharmaceutical Ingredients (APIs) / advanced intermediates. We have flexible business models to support various client needs.

01

End-to-end development

Process optimisation, technology transfer, validations and DMF filing followed by manufacturing upon commercialization.

02

Tech transfer & filings

Technology absorption, validations, DMF filing support and commercial manufacturing.

03

Commercial manufacturing

Technology absorption and commercial manufacturing for long-term supply partnerships.

To discuss a custom synthesis or CMO/CDMO partnership, please contact us.

Engineering & Feasibility Matrix

CDMO Project Feasibility & Capacity Estimator

Configure campaign parameters, reaction chemistry, and regulatory requirements to receive an instant facility allocation, reactor metallurgy match, and project timeline dossier.

1 Target Batch Scale / Campaign Volume
2 Key Reaction Chemistry / Metallurgy
3 Target Regulatory Standard

Real-Time Feasibility Dossier

Instant VPCL Engineering Match
Fully Feasible
Selected Scale & Chemistry Clinical / Pilot • Piperidone Synthesis
Allocated Manufacturing Facility Unit-I & Unit-III — Audited & Approved by USFDA
Assigned Reactor Metallurgy Glass-Lined Reactor (GLR) & Stainless Steel (SS316)
Estimated Tech Transfer Timeline 8 – 12 Weeks
Nominal Batch Size Capacity 10 – 100 kg
Regulatory Standard USFDA cGMP
Technical Infrastructure Notes Vasudha’s flagship core specialty with backwards-integrated raw material pipeline.

Direct Project Submission & CDA Request

Partner with a trusted API manufacturer

Whether you need high-quality APIs, intermediates or custom manufacturing support, our team is ready to collaborate.

Contact Our Team