Analytical Development & Validation Services

Analytical Development & Validation Services
Product Description

Seda provides comprehensive Analytical Development and Validation services to support pharmaceutical products from early development through clinical manufacture and regulatory submission.

Our analytical scientists develop, optimise, validate, and transfer robust analytical methods that ensure product quality, performance, and regulatory compliance. We support a wide range of activities including assay development, dissolution testing, impurity profiling, stability-indicating methods, degradation studies, and analytical troubleshooting.

Working closely with formulation, DMPK, modelling & simulation, and GMP manufacturing teams, we deliver analytical solutions that accelerate development timelines and reduce technical risk. Our model-informed approach enables data-driven decision-making throughout the product development lifecycle, supporting successful progression from concept to clinic.

SEDA Pharmaceutical Development Services

  • Country/Region:
    United Kingdom
  • Founded:
    2015
  • On CPHI since:
    2023
  • Certificates:
    1
  • Employees:
    50 - 99
Company types
CMO/CDMO
Contract Research Organisation (CRO)
Pharmaceutical company
Primary activities
Contract Research Organisation
Packaging & drug delivery
Specifications
  • Details
  • Analytical method development
  • Analytical method validation
  • Method transfer and verification
  • Stability-indicating methods
  • Dissolution method development
  • Impurity profiling
  • Degradation studies
  • Release and stability testing support
  • Regulatory compliance support
  • CMC analytical package generation
  • Selling Points
  • End-to-end analytical development and validation expertise
  • Stability-indicating method development
  • Regulatory-compliant analytical packages
  • Support for oral solid dosage and other drug products
  • Rapid analytical problem-solving and troubleshooting
  • Seamless integration with formulation and GMP manufacturing activities
  • Model-informed development approach
  • Experienced scientists with strong regulatory understanding
  • SEDA Pharmaceutical Development Services

    • Country/Region:
      United Kingdom
    • Founded:
      2015
    • On CPHI since:
      2023
    • Certificates:
      1
    • Employees:
      50 - 99
    Company types
    CMO/CDMO
    Contract Research Organisation (CRO)
    Pharmaceutical company
    Primary activities
    Contract Research Organisation
    Packaging & drug delivery

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