Contract Service
We are proficient in organic synthesis and process development of active pharmaceutical ingredients (APIs), intermediates and starting materials.
Our key areas of expertise include:
- Organic synthesis, heterocycles, carbohydrate chemistry, macrocycles, oligonucleotides, nucleosides, peptides,
- Chiral ligands, asymmetric synthesis and chiral separations.
- Heterogeneous catalysis,
- High potent APIs,
- Complex APIs,
- Identification and synthesis of impurities
- Crystallization and polymorphism,
- Characterization using analytical techniques.
- Process scale-up and technology transfer.
- Quality and Regulatory compliance
Our expertise can support in developing efficient and cost-effective synthetic routes and delivering products from milligram to kilogram quantities meeting the needs of different clients.
We offer services in the following areas to support research & development and manufacture of APIs, Intermediates and Key strating materials.
Custom Synthesis
We offer custom synthesis services in the following areas to support integrated drug discovery and development in the pharmaceutical industry.
- Synthesis of KSMs and Intermediates
- Synthesis of impurity standards
- API Reference standards
- Polymorph screening studies
We handle custom synthesis projects in different contract options such as purchase order (PO), fee for service (FFS) and fulltime equivalent (FTE) and flexible to work in collaboration as a trusted partner.
We look forward to your feedback on how we can help to meet your research objectives.
High Margin Intermediates and Specialty Chemicals
Based on customer/client requirement we can provide following services:
1. Pre Market Information
2. Lab process development
3. Scale-up & Technology Transfer
4. Commercial Manufacturing Support
Project Management Services
We provide strategic guidance and project management services, which includes:
• Creating project plans and defining objectives.
• Identifying external resources, vendors, and partners.
• Collaborating with Contract Research Organizations (CRO) and Contract Manufacturing Organizations (CMO).
• Conducting due diligence and overseeing project progress.
• Offering guidance on current Good Manufacturing Practices (cGMP) and ensuring regulatory compliance.
• Support on Chemistry, Manufacturing, and Controls (CMC) sections for regulatory submission documents such as Drug Master File and New Drug Application (NDA).
