Clinical, Technical & R&D Services

Comprehensive Clinical, Technical & R&D Services

Access comprehensive international data on clinical research, technical expertise, and research & development organizations supporting the pharmaceutical, biotechnology, and cosmetic industries.

Our platform provides verified information on CROs (Contract Research Organizations), CDMOs, analytical laboratories, and innovation centers operating under GCP, GLP, and GMP standards. Explore detailed data on clinical trials, bioequivalence studies, formulation development, stability testing, and technology transfer programs. With continuously updated clinical and R&D intelligence, you can identify qualified scientific partners, accelerate product innovation, and ensure regulatory compliance throughout the development and commercialization process.

Clinical Research Services

  • Clinical trial design and management (Phase I–IV)
  • Clinical monitoring and data management
  • Clinical protocol preparation and ethical approval submission
  • Bioavailability and bioequivalence (BA/BE) studies
  • Pharmacokinetic (PK) and pharmacodynamic (PD) studies
  • Clinical trial site management and investigator coordination
  • Clinical data analysis and statistical reporting
  • Contract research organization (CRO) services
  • Clinical pharmacology research and bio-study supervision
  • GCP (Good Clinical Practice) compliance audits
  • Preclinical research and molecule discovery
  • Toxicology and safety evaluation studies
  • CRO partnership and project outsourcing management
  • Regulatory submission and CTD technical file preparation

Technical Development Services

  • Formulation development for tablets, capsules, injectables, and topicals
  • Process development and scale-up from lab to pilot to production stage
  • Analytical method development and validation
  • Stability testing (accelerated and long-term)
  • Laboratory testing (chemical, microbiological, and physical analysis)
  • Dissolution and disintegration testing for dosage forms
  • API and excipient compatibility studies
  • Pilot batch production for R&D and registration purposes
  • Packaging material testing and compatibility evaluation
  • Method transfer and technology transfer services
  • Process validation and equipment qualification (IQ, OQ, PQ)
  • Development of modified-release and novel drug delivery systems (NDDS)
  • Lyophilization and sterile formulation development
  • Biosimilar and biotechnological product development

R&D Support & Consulting Services

  • Impurity profiling and reference standard preparation
  • R&D documentation and technical dossier writing (CTD, eCTD)
  • Analytical laboratory setup and calibration support
  • GLP (Good Laboratory Practice) compliance audits
  • Technology licensing and formulation optimization consulting
  • Product reformulation for stability improvement or cost reduction
  • Scale-up studies and process optimization for commercial manufacturing
  • Development of combination drugs and fixed-dose formulations
  • Technical training for R&D, QC, and production teams
  • Product lifecycle management and continuous improvement
  • Patent research and formulation differentiation studies
  • Documentation of analytical reports and validation protocols
  • Technical consultancy for new product pipeline planning
  • Quality by Design (QbD) implementation

Quality Standards & Compliance

🏥 Clinical Standards
  • Good Clinical Practice (GCP)
  • ICH Guidelines Compliance
  • Ethical Committee Approvals
  • Clinical Data Management Standards
  • Patient Safety Monitoring
🔬 Laboratory Standards
  • Good Laboratory Practice (GLP)
  • GMP Compliance for R&D
  • ISO 17025 Accreditation
  • Data Integrity (ALCOA+)
  • Method Validation Protocols

Strategic R&D Advantages

Accelerated Innovation

Leverage specialized expertise to accelerate product development and reduce time-to-market.

Regulatory Compliance

Ensure full compliance with GCP, GLP, and GMP standards throughout development lifecycle.

Cost Efficiency

Optimize R&D investments through strategic partnerships and efficient resource allocation.

Expert Knowledge

Access specialized scientific expertise and cutting-edge research methodologies.

We conduct comprehensive verification including GCP/GLP certification checks, facility audits, track record analysis, client reference validation, regulatory inspection history review, and continuous performance monitoring. All research partners must demonstrate proven expertise and maintain current regulatory compliance.

Yes, we provide comprehensive global clinical trial support with local expertise in each region. Our network includes clinical research organizations and sites across North America, Europe, Asia, Middle East, and Latin America, ensuring compliance with local regulations and ethical requirements.

We follow a structured technology transfer approach including knowledge transfer, process validation, analytical method transfer, documentation preparation, and staff training. Our methodology ensures seamless transition from R&D to commercial manufacturing while maintaining product quality and regulatory compliance.

Absolutely. We provide comprehensive regulatory support including clinical trial application preparation, ethics committee submissions, health authority communications, and ongoing regulatory compliance monitoring throughout the clinical development process.

We implement robust data integrity measures including electronic data capture systems, audit trails, source data verification, monitoring visits, statistical quality control, and compliance with ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, Available).
Our Services
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