Custom Synthesis
Custom Synthesis
Unlock Future with Custom Synthesis ---
Unlock Future Pharmaceutical Research with ISP Custom Synthesis
When your research requires unique pharmaceutical impurities that aren't commercially available, ISP's Custom Synthesis services are here to help. We provide tailored solutions that enable precise impurity quantification, expanding your research capabilities. Whether you're dealing with newly identified or complex impurities, our team can develop new synthetic routes or optimize existing ones, speeding up your contaminant research.
From custom reference compounds to impurities and stable labeled isotopes, ISP delivers the expertise you need to push the boundaries of pharmaceutical impurity research. Partner with us toaccelerate your discovery process and explore new possibilities.
What we offer
· Value added customized synthesis
. Expert project planning and management
. Development of new synthetic routes
. Milligram to kilogram batch synthesis capacity
. Fully developed purification and analytical capabilities
We offer synthesis of pharmacopeial and non-pharmacopeial Impurity standards including - Degradation Impurities, Process Impurities, Potential Impurities, KSM impurities, API impurities etc.
FAQs
FAQs – Custom Synthesis
- Our Process
Step
01
Consultation
- Discussion of the problem
- Decision on Time frame, quotation, and Delivery
- Once confirmed Confidentiality/ NDA given to the customer
Step
02
Synthesis
- Discussion on all possible synthetic routes
- Process research, development and optimization
- Trouble shooting
- Synthetic route design and optimization,
- Laboratory support and Timely updates on the progress to the customer
- Product Development
Step
03
QA and Delivery
- High standard QA
- Product delivery with strong CoA
- Product delivered with Custom packing on time
- Frequently asked questions
ISP Standards specializes in synthesizing pharmacopeial and non-pharmacopeial impurity standards, including degradation impurities, process impurities, potential impurities, KSM (Key Starting Material) impurities, and API (Active Pharmaceutical Ingredient) impurities.
We prioritize confidentiality through Non-Disclosure Agreements (NDAs) before project initiation. Additionally, our process involves high-standard QA, timely updates, and the delivery of products with a robust Certificate of Analysis (CoA) to ensure quality and transparency.
The process begins with a consultation to discuss the problem, timeline, and pricing. After confirming the project, we design synthetic routes, optimize the process, and keep customers updated with regular progress reports. Once synthesis is complete, products undergo quality checks and are delivered in custom packaging within the agreed timeline.