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...

Read full company description
Address: Stieffring 14, 13627, Berlin
Germany
Germany Local time:

Modern GMP facility

Team of academics and technical experts

Small to large batch sizes possible

Our clients:

All API buyers

Our services:

APIs

Response time:

Employees:
30+
Established in:
1982
Number of products Number of products:
7

CPL Sachse in the media

Wirkstoffe – Made in Germany (DE)

Wirkstoffe – Made in Germany (DE)

Learn more

Where we are located

Our products

Filters

Reset current filters

Selected filters:

Type
Production region
Country of origin
Qualifications

Producer

Produced in:

Germany

MOQ: 200 g

  • CoA

  • GMP

  • MSDS

  • FDA

  • EDMF/ASMF

Contact supplier

Replies quickly

Producer

Produced in:

Germany

MOQ: 500 g

  • CoA

  • GMP

  • MSDS

  • FDA

  • EDMF/ASMF

Contact supplier

Replies quickly

Producer

Produced in:

Germany

MOQ: 50 g

  • GMP

  • CoA

  • CEP

  • FDA

  • MSDS

  • BSE/TSE

Contact supplier

Replies quickly

Producer

Produced in:

Germany

MOQ: 500 g

  • GMP

  • CoA

  • CEP

  • FDA

  • MSDS

  • USDMF

Contact supplier

Replies quickly

Producer

Produced in:

Germany

MOQ: 500 g

  • CoA

  • GMP

  • FDA

  • MSDS

  • USDMF

  • EDMF/ASMF

Contact supplier

Replies quickly

Produced in:

Germany

MOQ: 6 kg

  • CoA

  • GMP

  • FDA

  • MSDS

  • EDMF/ASMF

Contact supplier

Replies quickly

There are 1 more products visible after logging in!

Login

Contact CPL Sachse and get a competitive price offer.

CPL Sachse is a supplier from Germany. They offer 7 products (APIs, Excipients or Intermediates). Contact CPL Sachse for free and get a competitive price offer.

Find a price of Anagrelide bulk with GMP, FDA offered by CPL Sachse.
Find a price of Atipamezole bulk with GMP, FDA offered by CPL Sachse.
Find a price of Clenbuterol bulk with GMP, CEP, FDA offered by CPL Sachse.
Find a price of Detomidine bulk with GMP, CEP, FDA, USDMF offered by CPL Sachse.
Find a price of Medetomidine bulk with GMP, FDA, USDMF offered by CPL Sachse.
Find a price of Phenoxybenzamine bulk with GMP, FDA offered by CPL Sachse.

Note that some products will only be visible after logging in.

Are you looking for pharmaceutical ingredients for the production of medicines? Contact the supplier of your choice by using the send inquiry button and find out how much it cost. The supplier will contact you with their price and conditions. CPL Sachse replies quickly.

You can send an inquiry for these products. Some suppliers have set a minimum order quantity (moq). Provide enough information regarding your enquiry. Let CPL Sachse know whether you are looking for Ph.Eur (EP), USP, BP, JP grade. Also, let the manufacturer or trader know if you are looking for hydrochloride (HCl), base or other product specifications. Is it for own production, resale or research purposes? Contact CPL Sachse, get a price, download certificates and buy the product.

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.