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Full-lifecycle CDMO · WHO-GMP & PIC/S certified

Contract manufacturing — reliable, scalable, certified

A trusted contract manufacturing partner for domestic and international brands — the full production lifecycle from raw material procurement and testing to bulk manufacturing, packaging, quality release and dispatch, under a single WHO-GMP and PIC/S certified roof.

WHO-GMP & PIC/STwo facilitiesAll four verticalsFlexible batch sizes
Single compliant roof
WHO-GMP certified
International manufacturing standard
PIC/S certified
Export-ready compliance regime
Two manufacturing facilities
Nalagarh & Paonta Sahib
All four verticals
Pharma · nutra · derma · injectables
One accountable partner

Everything under one compliant roof

Outsourcing production should remove complexity, not add it. Biodeal manages the entire lifecycle — raw material procurement and quality testing, bulk manufacturing, packaging, quality release and dispatch — so a brand answers to one accountable partner rather than coordinating a chain of vendors.

With two manufacturing facilities and capability across all four product verticals, flexible batch sizes suit brands at every stage — from a careful market introduction to high-volume commercial production. The WHO-GMP and PIC/S certified quality system is the same whichever vertical, volume or destination market you build for.

01

Single certified roof

WHO-GMP & PIC/S compliance across procurement, manufacture, packaging and release.

02

Scales with you

Flexible batch sizes from market-introduction runs to high-volume commercial supply.

03

Four verticals

Pharmaceuticals, nutraceuticals, derma & cosmetics and injectables on one system.

What's included

Seven elements, one supply contract

Each engagement covers the full production lifecycle — from supplier qualification through to compliant dispatch — backed by complete documentation at every step.

01

Dedicated production lines

Separate lines per product category — preventing cross-contamination and ensuring schedule reliability.

02

Raw material sourcing & testing

Supplier qualification, incoming material testing and Certificate of Analysis verification.

03

Manufacturing & in-process QC

GMP-compliant production with in-process quality controls and batch manufacturing records.

04

Regulatory dossier support

CTD/ACTD dossier preparation and product registration support for domestic and export markets.

05

Packaging & labelling

Full packaging design coordination, serialisation and labelling compliance support.

06

On-time delivery

Batch scheduling and supply-chain management for reliable, predictable delivery timelines.

07

Compliance documentation

WHO-GMP & Schedule M compliance documentation for all regulatory requirements.

How engagement works

From first brief to first dispatch

A clear, four-step path takes a programme from initial enquiry to repeatable commercial supply — with a routed proposal in the first 48 hours.

WHO-GMP
& PIC/S certified roof
2
Manufacturing facilities
4
Product verticals served
48h
To a routed proposal
01

Scope & proposal

Share product category, dosage form, target markets and approximate volumes — we respond within 48 hours with capacity availability and a preliminary manufacturing proposal.

Within 48 hours
02

Technical transfer

Formulation, specifications and analytical methods are transferred and qualified; raw materials and suppliers are sourced and tested against agreed standards.

Tech transfer & sourcing
03

Validation & pilot

Dedicated lines are validated and pilot batches manufactured under in-process QC, with dossier and registration support prepared for the destination markets.

Validation & dossier
04

Commercial supply

Full commercial production with quality release, packaging, serialisation and on-time dispatch — backed by complete WHO-GMP & Schedule M documentation.

Quality release & dispatch
FAQ

Contract manufacturing, answered

The questions brands ask most often when choosing a contract manufacturing partner.

What is pharmaceutical contract manufacturing?

Contract manufacturing (also called third-party manufacturing) is when a pharmaceutical brand outsources production to a certified manufacturer. The brand owns the product formula and marketing rights; the manufacturer handles production and quality. A CDMO like Biodeal also provides development services alongside manufacturing.

How do I start contract manufacturing with Biodeal?

Submit an enquiry via the contact form specifying product category, dosage form, target markets and approximate volumes. Biodeal's team will respond within 48 hours with capacity availability and a preliminary manufacturing proposal.

What is the difference between contract manufacturing and a CDMO?

A contract manufacturer produces to a client's specification. A CDMO provides both development services (formulation R&D, stability studies, regulatory dossiers) and commercial manufacturing — making Biodeal a complete partner from early development through commercial scale-up.

Start the conversation

Request a manufacturing proposal

Tell us your product category, dosage form, target markets and approximate volumes — our CDMO team responds with capacity availability and a preliminary manufacturing proposal within 48 hours.

Request a manufacturing proposal Speak with our CDMO teaminfo@biodealpharma.com · +91 120-6025048