Our Services | Pinak Corporation

what we offer

End-to-End Pharma Solutions

From contract manufacturing to regulatory dossier preparation and global sourcing — we deliver comprehensive services across the pharmaceutical value chain.

Manufacturing

Contract Manufacturing

We offer manufacturing of your products and your brands on contract basis — hence clients no longer need to have their own factories to launch their own brands/products. We handle the entire responsibility of manufacturing, enabling client companies to focus on their core competence of marketing.

End-to-end manufacturing responsibility
Focus on marketing while we handle production
Quality assured manufacturing processes
Flexible production capacities

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Contract Manufacturing

Pharmaceuticals Export

Export

Pharmaceuticals Export Services

We offer international customers access to Brand and Quality Generics for popular drugs from reputed Indian Pharmaceutical Companies which have been investing significantly in R&D. Reliable, compliant, and cost-effective.

Access to Brand and Quality Generics
From reputed Indian pharmaceutical companies
Reliable and compliant supply chain
Cost-effective solutions

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Sourcing

Product Sourcing

We provide comprehensive product sourcing services to help you find the right products at the right price from the right partners.

Sourcing of the right product from the right company at the right price
Taking care of all required legal formalities and documents
Regulatory affairs and follow up for documents
Supply chain aspects, lead time management & follow up for timely dispatch
Quality assurance

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Product Sourcing

Regulatory Affairs

Regulatory

Regulatory Affairs

Our regulatory affairs team ensures your products meet all compliance requirements for global markets.

Dossier Compilation & Submission (CTD, ACTD, eCTD, NeeS, country specific)
CTD / ACTD dossier writing & auditing
BA/BE Studies & Clinical Trials (DCGI & BE NOC)
DMF / ASMF writing
Analytical Method Validation & Impurity Profile

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Transfer

Technology Transfer

Our technology transfer services ensure seamless knowledge transfer and process implementation across your organization.

Centralized governance and decision making
Quality assurance and regulatory alignment
Gap analysis and risk management
Communications, documentation systems & supply-chain
Project management & process knowledge codification

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Technology Transfer

Dossier Preparation

Dossier

Dossier Preparation & Management

We provide comprehensive dossier preparation and management services to streamline your regulatory submissions.

CTD Dossier Compilation, Submission, Writing, Auditing
Conversion: Non-CTD → CTD, CTD → eCTD, ACTD, NeeS
Clinical trial report writing & DCGI applications
ACTD compilation for ASEAN, CIS & other markets

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RLD / Innovator

Reference Listed Drugs (RLDs)

We supply Reference Listed Drugs and innovator samples essential for bioequivalence studies and clinical trials.

Comparator drug sourcing & innovator samples supply
Essential for bioequivalence studies & clinical trials
Regulatory compliance & quality assurance
Ensuring safe and effective medications

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Reference Listed Drugs

Named Patient Pathways

Patient Access

Named Patient Pathways

For patients who have run out of options, are awaiting new therapies, or urgently need hard-to-find medicines — we ensure safe and compliant access to unlicensed medicines. In close collaboration with hospitals, pharmacies, and regulators, we bridge critical care gaps when time matters most.

Safe and compliant access to unlicensed medicines
Collaboration with hospitals, pharmacies, and regulators
Bridging critical care gaps
Time-sensitive patient access solutions

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Ready to Partner With Us?

Let's discuss how we can support your pharmaceutical, nutraceutical, or cosmetic needs.