Syngene - Contract Research Organization
 
About SyngeneChemistry Research Services Biology Research Services IPR Infrastructure Career at Syngene
Analytical Services
  > CHEMISTRY
  Overview
  Medicinal Chemistry
  Library Synthesis
  Process R&D
  Custom Manufacturing
  Analytical Services
  Polymer Chemistry
  
  Home
  
  
 
  
     
  Analytical Services

Methods Development Services

To develop and optimize methods, scientists at our cGMP compliant analytical facilities are equipped with an array of tools and techniques, including HPLC, LC-MS/MS, TLC, GC and GC/MS.

Syngene develops analytical methods for the following applications:

- Potency
- Impurities
- Residual solvents
- Physical and chemical tests
- Cleaning assessment
- Chiral purity
- Others as requested


Validation Services

After a successful method development, Syngene has the capabilities to validate analytical method as per ICH guidelines. Our analysts frame their methods validation activities using a practical approach coupled with outstanding quality and sound scientific expertise.


Analytical Method Validation is categorized as below:


Chromatographic Method Validation

HPLC
  - Assay of actives
  - Related compounds or impurities
  - Cleaning validation
  - Preservatives or Major excipients

GC
  - Residual solvents by headspace GC

Non-chromatographic Method Validation

  - Titrimetric assay methods
  - TLC related substance methods
  - UV assay methods


Typical characteristics include:

- Specificity
- Forced degradation or Stress study
- Oxidative
- Base
- Acid
- Photolytic
- Thermal
- Limit of detection
- Limit of quantitation
- Range (Accuracy, Linearity and Precision)
- Ruggedness or Intermediate precision
- Robustness
- Solution stability (Standard and Sample)
- Response factor determination


Steps in Analytical Method Validation (For external methods):

- Method Assessment/Evaluation for external methods
- Method optimization or modification (if required)
- Method development undertaken if existing methods are not   specific
- Pre-validation assessment prior to approval of validation   protocol
- Validations undertaken after protocol approval
- Protocol has sign off from both Syngene and clients QA.
- Post experimental validation report is written at Syngene
  Report is reviewed and approved by QA (Syngene and Client’s)


Stability Studies

Syngene offers stability studies as an integral component of its analytical services.


Stability Testing

- APIs
- R&D preliminary stability (protocol development, testing and   evaluations)
- QC release/stability


Stability Storage

- Walk-in/Reach-in units
- ICH conditions
- Continuous monitoring
- Continuous alarming
- Generator back-up
- IQPQ with mapping


Stability Reporting

- 4-week reporting windows
- Data trending
- Comprehensive reports
 
     
Analytical Method Development & Validation
  Related links:
    Facilities
    Confidentiality
    Accreditations
    Job Opportunities
 
Home  |  Contact Us  |  Site Map

Arogya Raksha Yojana | Biocon Foundation | ABLE | Karnataka Vision Group on Biotechnology | Karolinska Institute
 
  * Disclaimer | Related Links © 2011, Syngene. All Rights Reserved