-
First text 2
-
First text 3
-
First text 3
-
First text 3
Our Services
- Route selections
- Process development, optimizations & validations
- Multi step synthesis
- Library synthesis
- Reference material development
- Custom synthesis from mg to gram level
- Method development
- Method validation
- Isolation and purification of Reference standards of main synthetic compounds and Impurities.
- Isolation and purification of Reference standards of natural compounds and Impurities.
To develop and optimize methods, scientists at Crams Technologies cGMP compliant analytical facilities are equipped with an array of tools and techniques, including HPLC, GC and TLC etc. Crams Technologies develops analytical methods for all the analytical applications such as:
- Potency
- Impurities
- Residual solvents.
- Physical and chemical tests.
- Cleaning assessment.
- Chiral purity.
After a successful method development, Crams Technologies has the capabilities to validate analytical method as per ICH guidelines. Our scientists perform methods validation activities using a practical approach coupled with outstanding quality and sound scientific expertise.
We will perform validations for chromatographic as well non chromatographic as well non chromatographic methods as per regulatory requirements and mutually agreed protocols. At Crams Technologies, stability studies are a part of its analytical services.
- Dossier preparation
- DMF compilations
- ANDA compilations
- Due Diligence
- Third Party audits
- Strategies for Pharma organizations
- Patent Search & Literature Back-up
- Infringement analysis support
- Patent Drafting
