Pharmaceutical Formulation Research & Development (FR&D) Services
Comprehensive pharmaceutical formulation development services supporting product development from concept to commercial launch across global markets.
FR&D Services
PHARMULA provides a complete range of Formulation Research & Development (FR&D) services required to support customers from early-stage product development to commercial launch within the best achievable timelines.
Our integrated approach makes us a true one-stop solution for pharmaceutical formulation development, ensuring quality, compliance, and scalability for any market.
Galenic Development
Our Galenic Development services focus on building robust and effective pharmaceutical formulations through scientific and process-driven approaches.
Scope of Galenic Development Includes:
- Selection of appropriate pharmaceutical dosage form
- Compatibility studies of active substances and excipients
- Definition of qualitative and quantitative formulation composition
- Design of manufacturing methods
- Establishment of process controls
- Technology transfer to the client
Analytical Development
PHARMULA offers comprehensive analytical development services to ensure product quality, safety, and compliance throughout the development lifecycle.
Analytical Development Services Include:
- Development and validation of analytical methods
- Control of active substances, impurities, and degradation products
- Raw material and finished product analysis
- In-vitro diss olution testing
- Cleaning validation support
- Microbiological control
Stability Studies
We conduct stability studies to evaluate the performance and shelf-life of pharmaceutical products in line with global regulatory expectations.
Stability Study Services Include:
- Pre-stability studies during drug product development
- Stability studies as per ICH guidelines
- In-use stability studies
- Photostability studies
- Post-marketing stability studies
Regulatory Services (Fr&D Support)
PHARMULA provides regulatory services integrated with FR&D activities to support product registration and compliance.
Regulatory Support Includes:
- Compilation of drug product dossiers
- eCTD and CTD format documentation
- Orphan drug designation management
- Investigational Medicinal Product Dossier (IMPD) support
Manufacturing Of Pilot & Clinical Trial Batches
We conduct stability studies to evaluate the performance and shelf-life of pharmaceutical products in line with global regulatory expectations.
PHARMULA supports the manufacturing of pilot and clinical trial batches through partner facilities that comply with cGMP requirements, particularly for injectable formulations.
This ensures consistency between development, scale-up, and commercial manufacturing stages.
Comprehensive Fr&D Services Under One Roof
PHARMULA’s FR&D services are supported by carefully selected business verticals that address key challenges of the pharmaceutical industry:
Contract / Custom Development Organization (CDO)
Contract Manufacturing Services (CMO)
Process Development & Technology Transfer (PDTT)
Contract Development & Manufacturing Organization (CDMO)
Expert Consultancy Services
What Makes Pharmula A One-Stop Fr&D Partner
Integrated FR&D services from concept to commercial readiness
Strong alignment between development, manufacturing, and regulatory needs
Scientifically driven and compliance-focused approach
Scalable solutions for any market
Experienced team supporting end-to-end pharmaceutical development
Who This Service Is For
- Pharmaceutical companies developing new formulations
- SMEs without in-house R&D capabilities
- Companies planning product registration in global markets
- Businesses seeking end-to-end formulation development support
Engagement Models
Contract or custom formulation development
Joint development or mutual business models
Sponsored development programs
Integrated FR&D with manufacturing and regulatory coordination
