CDMO Services - Contract Development & Manufacturing | DRK Research Solutions SA
CDMO Services

From Concept to Commercial - Integrated Drug Development & Manufacturing

DRK Research Solutions SA is your end-to-end CDMO partner. We advance pharmaceutical and biopharmaceutical products from early formulation through process validation, regulatory submission, and global commercial supply - with Swiss quality and global execution.

"At DRK, we don't just work for you - we work with you; combining Swiss quality with global agility to deliver excellence without exception."
DRK Research Solutions SA
Pharmaceutical scientist in laboratory
GMP-Certified Manufacturing Swiss quality · Global execution
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Expert Professionals
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Therapeutic Areas
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Regulatory Markets
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Global Offices
Core CDMO Capabilities

Everything Your Product Needs, Under One Roof

Our fully integrated CDMO platform eliminates the complexity of working across multiple vendors. From lab-scale development to commercial batch manufacturing, DRK provides seamless continuity at every stage.

Pharmaceutical formulation laboratory
01 - Development

End-to-End Product Development & Manufacturing

Seamless advancement from early-stage formulation through process validation, regulatory submission, and commercial manufacturing with accelerated time to market.

FormulationScale-UpTech Transfer
Scientific documentation technology transfer
02 - Technology Transfer

Lab-Scale Development & Technology Transfer

Fully documented transition of data, materials, and process know-how to partner sites - safeguarding product integrity and long-term supply reliability.

Analytical MethodsDocumentation
Strategic pharmaceutical partnership agreement
03 - Partnerships

Out-Licensing & Strategic Partnerships

Three flexible models: out-licensing with commercial supply, complete technology transfer, or a ready-to-submit regulatory dossier - tailored to your investment objectives.

Out-LicensingCo-Development
GMP pharmaceutical manufacturing facility
04 - Manufacturing

Commercial Contract Manufacturing & Supply

Consistent, GMP-compliant manufacturing from engineering batches through full commercial-scale production - ensuring uninterrupted global supply.

GMP CompliantScalableGlobal Supply
Clinical trial supply vials packaging
05 - Clinical Supplies

Clinical Trial Supplies

Comprehensive IMP development, GMP clinical manufacturing, customised packaging, and integrated logistics across all clinical trial phases globally.

IMPGMPGlobal Logistics
Regulatory affairs documentation review
06 - Regulatory

Regulatory Strategy & Market Access

Comprehensive support across EMA, USFDA, MHRA, EAEU, and WHO - eCTD dossiers, bioequivalence coordination, and post-approval lifecycle management.

EMAUSFDAMHRAeCTD
Development Pathway

A Proven, Stage-Gated Process From Concept to Commercial

Every milestone is documented, reviewed, and approved before the next phase begins. Nothing is left to assumption - every decision is backed by data and multidisciplinary expert review.

Stage 01

Pre-Formulation Studies & Literature Review

Stage 02

Lab-Scale Formulation Development & Optimisation

Stage 03

Analytical Method Development & Validation

Stage 04

Process Development

Stage 05

Container Closure System Qualification

Stage 06

Technology Transfer to Manufacturing Site

Stage 07

Engineering & Exhibit Batch Manufacturing

Stage 08

Process Validation & Cleaning Validation

Stage 09

Stability Studies

Stage 10

Regulatory Dossier Compilation & Submission (eCTD Modules 2-5)

Stage 11

Commercial Manufacturing & Supply

Pharmaceutical process validation scientist
Stage-Gated Development Each milestone reviewed and approved before advancing - scientific governance and multidisciplinary oversight at every step.
Therapeutic Expertise

Deep Formulation Expertise Across Eleven Therapeutic Categories

Our scientific team brings focused capability in complex generics, niche products, and hybrid 505(b)(2) formulations across key therapeutic areas.

Pharmaceutical research scientist at work

"DRK's scientific team brings deep formulation, analytical, and regulatory expertise across key therapeutic categories - with focused capability in complex generics and niche products."

Anti-Infectives

Antibacterial, antiviral, antifungal agents

CNS

Antipsychotics, antidepressants, anxiolytics

Dermatology

Acne, psoriasis, eczema therapies

Gastroenterology

GERD, IBD, IBS, anti-emetics

Metabolic Disorders

Diabetes, dyslipidemia, obesity

Nutritional

Vitamins, probiotics, immunity boosters

Oncology

Solid tumours, haematological malignancies

Ophthalmology

Glaucoma, dry eye, post-surgical care

Pain & Inflammation

NSAIDs, analgesics, rheumatology

Respiratory

Asthma, COPD, allergic rhinitis

Women's Health

Maternal, reproductive, general wellness

Emerging Focus

DRK is actively developing capability in monoclonal antibodies (mAbs), recombinant proteins, CAR-T therapies, and gene therapy - positioning for next-generation biologics programmes.

Dosage Form Capabilities

Specialised Manufacturing Across Complex Dosage Forms

We combine scientific depth with integrated manufacturing capabilities - solving technical challenges and aligning each dosage form with its regulatory and commercial objectives.

Oral solid dosage forms tablets and capsules

Oral Solids

  • Immediate & modified release tablets
  • Effervescent & enteric coated tablets
  • Chewable tablets
  • Hard & soft gelatin capsules
  • Sachets, stick packs
  • Paediatric age-appropriate forms
Sterile injectable pharmaceutical vials

Liquids & Semi-Solids

  • Solutions, suspensions, syrups, drops
  • Sterile injectables (vials & ampoules)
  • Ophthalmic solutions & suspensions
  • Preservative-free unit-dose systems
  • Topical creams, ointments, gels
  • Dermal sprays and foams
Inhaler and respiratory drug delivery devices

Specialised Delivery Systems

  • Dry Powder Inhalers (DPIs)
  • Metered Dose Inhalers (MDIs)
  • Nasal sprays
  • 505(b)(2) hybrid formulations
  • New strengths & routes of administration
  • Orphan & rare disease programmes
Why DRK

The CDMO Partner Built for Global Markets

DRK combines scientific expertise, regulatory intelligence, and agile project execution to deliver fully integrated CDMO solutions that reduce complexity and accelerate products to commercialisation.

Swiss Excellence, Global Execution

Internationally benchmarked quality standards delivered across global markets.

Flexible Engagement Models

Customised structures aligned with your programme stage and commercial objectives.

Accelerated Time-to-Market

Milestone-driven execution minimising timeline risk with full regulatory compliance.

Multi-Regulatory Expertise

Streamlined multi-market submissions through a single fully integrated partner.

Supply Chain Resilience

Proactive sourcing strategies ensuring uninterrupted product supply globally.

Risk & Project Governance

Stage-gated development with documented decision points and full transparency.

Pharmaceutical quality control scientist cleanroom
Quality Without Compromise GMP-certified processes aligned with international regulatory standards
Global Reach

Regulatory Expertise Across Key Global Markets

Active regulatory intelligence and dossier expertise across major global authorities - enabling sponsors to pursue multi-market approvals through a single integrated development partner.

EMAUSFDAMHRA (UK) EAEUWHOEU Markets MENA RegionAPAC MarketsEmerging Markets
Global pharmaceutical regulatory team
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Ready to Advance Your Programme

Whether you are at pre-formulation stage or seeking a commercial manufacturing partner, our team of over 100 experts is ready to develop a solution tailored to your programme's specific requirements and timelines.

Global offices: Geneva (HQ) · Cambridge, UK · Virginia, USA · Lahore, Pakistan · Kuala Lumpur, Malaysia · Kathmandu, Nepal · Dubai, UAE

Request a Proposal

Tell us about your programme. We respond within one business day.

DRK Research Solutions SA - Chem. de la Blonde 38, 1253 Vandoeuvres, Geneva, Switzerland · info.ch@drkresearch.com · +41 22 575 27 35