Services

Accelerate Pharma Success with Global-Ready Solutions

We provide comprehensive pharma lifecycle support — from regulatory strategy and dossier development to sourcing, scale-up, and commercialization — helping you bring high-quality products to market faster, smarter, and fully compliant.

Comprehensive pharma lifecycle support: from concept to commercialization
Global regulatory experience: FDA, EMA, ANVISA, NMPA
Global sourcing & logistics hubs in India, China, and Switzerland

Our Services

End-to-End Pharmaceutical Support — From Molecule to Market

We offer a comprehensive suite of services designed to support pharmaceutical and nutraceutical companies across every stage of their development. Whether you're sourcing APIs or excipients, navigating regulatory requirements, or managing complex logistics, our team ensures efficiency, compliance, and peace of mind at every step.

Regulatory Affairs & Documentation Support

We assist manufacturers with the review, and submission of all essential regulatory documents. Our team works closely with both suppliers and clients to ensure seamless registration in line with the specific regulatory standards of your country.
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Product Qualification & Technical Guidance

Our technical experts help evaluate the compatibility and quality of ingredients through prequalification, stability support, and analytical data review. We bridge the gap between manufacturer capabilities and client expectations through deep product knowledge and scientific collaboration.

Supply Chain & Logistics Management

With decades of experience and strong local partnerships, we manage sourcing, documentation, and delivery with efficiency and reliability. We ensure timely shipments, inventory planning, and regulatory-compliant distribution — so you stay on schedule, every time.

Strategic Sourcing & Global Supplier Network

Our sourcing hubs across different locations connect clients with certified, audited manufacturers. We prioritize quality, transparency, and long-term reliability to ensure product continuity and compliance with evolving market regulations.

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Regulatory Affairs

Navigate global compliance with confidence.

End-to-end support for CEP, CTD, ANDA, MAH, and IND submissions
Dossier gap analysis, enhancement, and formatting
Post-approval lifecycle management & vigilance
Regulatory consulting, due diligence & in-house team training
Expertise across global frameworks: FDA, EMA, ANVISA, NMPA

Regulatory Dossier Preparation

(CTD, ACTD, CADIFA, etc.)
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Country-specific registration support

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CEP application and updates

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78%

Dossier Co-Development

With an 85% success rate in dossier development, we help brands enter even the most challenging markets — including Brazil.

46%

Planning Projects

Nearly half of companies stumble at the planning stage — we guide and support brands to ensure successful product launches.

Our ServiceS

Flexible Pharma Partnerships

Collaborate with us to co-create long-term value.

Contract Manufacturing

Full-spectrum contract manufacturing & CDMO solutions.Comprehensive development-to-delivery support for oral, topical, injectable, and complex dosage forms.

Private label manufacturing

Private Labelling.Ready-to-launch product lines under your brand, with regulatory-ready documentation and flexible MOQs.

Packaging and Development

Packaging, Development & Customisation. Functional and compliant packaging solutions tailored for stability, branding, and regulatory needs.