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Anagrelide from CPL Sachse

We are an established order and contract manufacturer of active pharmaceutical ingredients (drug substances) and selected intermediates ranging from milligrams to kilograms. Our production follows cGMP and is in accordance with the EU-GMP-Guideline Part II (ICH Q7). We are regularly inspected by the responsible local authority which issues us with drug substance-specific GMP certificates. We are currently manufacturing nine certified APIs for market supplies exclusively for our customers on a regular basis.

 

Synthesis development

We have more than 30 years of experience in the development of organic syntheses for drug substances (APIs). On receipt of an order for synthesis development, we first research the latest state-of-the-art and conduct a feasibility study if applicable. This includes the proposed synthetic route, a schedule, and...

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Address: Stieffring 14, 13627, Berlin
Germany
Germany Local time:

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Modern GMP facility

Team of academics and technical experts

Small to large batch sizes possible

Our clients:

All API buyers

Our services:

APIs
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Producer

Produced in:

Germany

MOQ: 200 g

  • CoA

  • GMP

  • MSDS

  • FDA

  • EDMF/ASMF

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CPL Sachse Anagrelide API Producer - 68475-42-3

Description:
CPL Sachse offers high-quality Anagrelide API, certified for compliance with international standards. Manufactured in Germany. Modern GMP facility. Team of academics and technical experts. Small to large batch sizes possible.

Product Details

Certifications
CoA, GMP, MSDS, FDA, EDMF/ASMF compliant
Minimum Order Quantity
200 g
Produced in
Germany (Europe)
DrugBank ID
DB00261
CAS Number
68475-42-3
Unique Ingredient Identifier
K9X45X0051
Raw Material Category
Platelet Aggregation Inhibitors

Ordering Process

1. Inquiry Submission: Click "Send Inquiry" to connect directly with producer.

2. Requirement Specification: Outline your needs for tailored offers.

3. Quotation: Receive the best quote and terms exclusively through Pharmaoffer.

Additional Products

We offer 6 other Active Pharmaceutical Ingredients and excipients, showcasing our production and distribution capabilities.

Contact Us

Are you looking for Anagrelide API? Contact CPL Sachse by using the send inquiry button. We will respond quickly with pricing and terms exclusively through Pharmaoffer.

Please, provide enough information regarding your inquiry. Let us know whether you require Ph.Eur (EP), USP, BP, JP grade, whether you are looking for hydrochloride (HCl), base, or other specific product specifications. Additionally, please inform us if the API is intended for your own production, resale, or research purposes. Contact us to receive a quote, download certificates, and purchase the Anagrelide API

CPL Sachse

We are an established order and contract manufacturer of active pharmaceutical ingredients (drug substances) and selected intermediates ranging from milligrams to kilograms. Our production follows cGMP and is in accordance with the EU-GMP-Guideline Part II (ICH Q7). We are regularly inspected by the responsible local authority which issues us with drug substance-specific GMP certificates. We are currently manufacturing nine certified APIs for market supplies exclusively for our customers on a regular basis.

 

Synthesis development

We have more than 30 years of experience in the development of organic syntheses for drug substances (APIs). On receipt of an order for synthesis development, we first research the latest state-of-the-art and conduct a feasibility study if applicable. This includes the proposed synthetic route, a schedule, and a cost estimate for the execution of the necessary development work. It may also include an estimate of the future manufacturing costs for the drug substance.

 

Analytical development

In addition to the synthesis and drug development, we offer a comprehensive range of analytical services (incl. stability testing). Our range includes both routine analyses according to pharmacopoeial methods as well as the development of new analytical methods for drug substances and drug products. We have many years of experience in using gas chromatography (GC/MS, GC/FID) to determine residual solvents in pharmaceutical ingredients, drug substances (APIs), and drug products.