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CDMO-CMO


API production

Plants in:

India

Established in: 1989

Production scale:

large

Employees: 5000+

6 production facilities approved by USFDA, AGES-Austria, PMDA, WHO

R&D Centers with capabilities of ANDAs, DMFs and NDDS

462+ patents filed for drug substances and polymorphs

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

  • fda

Replies quickly

Plants in:

China

Established in: 2008

Production scale:

large

medium

Employees: 300+

More than 150 patents based on independent intelligence

Expertise in anti-tumor, anti-diabetes and cardiovascular API and intermediates.

GMP facility with annual production capacity of 300M

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

Replies quickly

CDMO-CMO


API production

Plants in:

India

Established in: 2021

Production scale:

small

Employees: 19

API, Intermediates, Building Blocks, Impurities, Amino acids and Peptides

Small quantity APIs to commercial scale

GMP and USFDA certification based on quantity, order, assignment.

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

  • fda

Replies quickly

Located in:

China

CDMO-CMO


API production

Plants in:

China

Production scale:

small

medium

large

Established for 17 years and a leading enterprise in China's API industry

Mature technology and advanced production equipment

Quality assurance and fast delivery

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

Replies quickly

CDMO-CMO


API production

Plants in:

Switzerland

Established in: 1964

Production scale:

small

medium

large

Employees: 135+

Market leader in Switzerland

Small and medium batch sizes

Pharmaceutical raw materials with a herbal or synthetic basis

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

Replies quickly

CDMO-CMO


API production

Plants in:

Germany

Established in: 1886

Production scale:

medium

small

Employees: 275+

Raw materials, CMO and OTC products

Two GMP certified locations

Customisable (small-sized) packages

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

  • fda

Replies quickly

Located in:

Germany

CDMO-CMO


API production

Plants in:

Germany

Established in: 1997

Production scale:

small

medium

Employees: 200

Top-tier adherence to global pharmaceutical standards including GMP, FDA and EMA

Advanced Chemistry Labs specialized in HP APIs, steroids, and peptides

Comprehensive analytical services to meet precise client specifications.

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

  • fda

  • ema

Replies quickly

CDMO-CMO


API production

Plants in:

China

Established in: 1987

Production scale:

medium

small

large

Employees: 50+

ISO 9001:2015 & SGS audited supplier

One-stop CDMO Solutions for APl and Key intermediates

Specialized in APIs & Pharmaceutical Intermediates for 37 years

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

Replies quickly

CDMO-CMO


API production

Plants in:

Germany

Established in: 1980

Production scale:

medium

Employees: 30+

EU-GMP and DIN EN ISO 9001:2015

Pioneer in the fractionation of sheep plasma

Pure & sterile high-quality products

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

Replies quickly

Plants in:

China

Established in: 2017

Production scale:

large

small

medium

Employees: 200+

Manufacturing facility approved by FDA and GMP certified

Obtained CNAS laboratory accreditation certificate

Subsidiary of the US listed group Amphastar Pharmaceuticals

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

  • fda

Replies quickly

CDMO-CMO


API production

Plants in:

Poland

Established in: 1951

Production scale:

medium

Employees: 455+

Largest Polish manufacturer of pharmaceuticals and a leader of the Polish pharmaceutical market.

FDA approved european manufcaturing facilities

Export APIs to more than 60 countries worldwide

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

  • fda

Replies quickly

CDMO-CMO


API production

Plants in:

Latvia

Established in: 1972

Production scale:

medium

Employees: 1,000+

EU-GMP for APIs and CEP for certain APIs

Exporting to over 50 countries worldwide

Long-standing technological advantage in adamantane, quinuclidine and nitrofurane chemistry

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

  • fda

Replies quickly

CDMO-CMO


API production

Plants in:

FranceBelgium

Established in: 1952

Production scale:

small

medium

large

Employees: 550+

API manufacturing (Innovators, Generics and Highly Potent)

A tailor-made and flexible service approach

State-of-the-art analytical services including solid form and QbD laboratories

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

  • fda

Replies quickly

CDMO-CMO


API production

Plants in:

ItalyPortugal

Established in: 1993

Production scale:

small

medium

large

Employees: 600

Integrated innovative platforms for Technology Transfer (TT&GO®)

Fermentation, purification, and chemical synthesis technologies on the same site

Scalability from Laboratory and Pilot to Industrial scales

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

  • fda

  • ema

Replies quickly

Plants in:

China

Established in: 2014

Production scale:

small

medium

large

Employees: 1000+

22 years of production experience

6 workshops and 9 production lines which has 100t/month production capacity

4 USDMFS & 5 CEPS & 200+ Patents

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

Replies quickly

CDMO-CMO


API production

Plants in:

China

Established in: 2013

Production scale:

medium

Employees: 25+

ISO9001 certified

Drug R&D center (in Hangzhou)

From lab scale (mg/g) to commercial scale (kgs/tons)

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

Replies quickly

Located in:

Germany

Plants in:

Germany

Established in: 1982

Production scale:

small

Employees: 30+

Modern GMP facility

Team of academics and technical experts

Small to large batch sizes possible

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

  • fda

Replies quickly

Looking for CMO/CDMO Services?

Find a list of providers specializing in CMOs/CDMOs Services for API. Navigate through our extensive selection to identify the supplier that aligns with your specific needs.

Pharmaoffer makes it easy and convenient to send inquiries at no cost. Directly connect with your chosen supplier and take the first step towards fulfilling your pharmaceutical needs easily and efficiently.

CMO/CDMO - Contract (Development) Manufacturing Organizations

CDMOs and CMOs are pivotal in the pharmaceutical and biotech industries, offering specialized services in drug development and manufacturing. They assist in scaling up production from laboratory to commercial quantities, while adhering to strict regulatory standards. These organizations play a crucial role in the efficient and cost-effective production of medical and pharmaceutical products, ensuring quality and compliance at every stage.

Ingredient

Ingredient CMOs/CDMOs specialize in the production of individual pharmaceutical ingredients, also known as active pharmaceutical ingredients (APIs) or drug substances. Their primary role is to synthesize, purify, and supply these chemical compounds in compliance with stringent quality standards.

API

APIs are the core of pharmaceutical products, determining the therapeutic efficacy. Their production involves complex synthesis, purification, and characterization processes, adhering to stringent regulatory standards. APIs are crucial in drug development for diverse medical conditions.


Pharmaoffer presents a comprehensive selection of Contract Development and Manufacturing Organizations (CDMOs) specializing in the production of Active Pharmaceutical Ingredients (APIs). Our platform caters to pharmaceutical professionals seeking expert services in API development and manufacturing, including API Manufacturing and API CDMO capabilities.


Key Services Provided by Our Listed CDMOs:


  • Complex Synthesis Capabilities: Expertise in intricate chemical synthesis processes, ensuring the production of high-quality APIs. This is a critical aspect of API production.

  • Rigorous Purification Processes: Advanced purification techniques to meet the highest purity standards essential for API efficacy and safety.

  • Detailed Characterization and Analysis: Thorough API characterization to ascertain structural integrity, stability, and compliance with pharmacopeial standards.

  • Compliance with Regulatory Requirements: Strict adherence to global regulatory guidelines, including FDA and EMA standards, ensuring the delivery of APIs that meet all necessary regulatory criteria.

  • Custom API Development: Tailored solutions for API development, catering to diverse therapeutic needs and specific drug formulations. This service is particularly important in the realm of Active Pharmaceutical Ingredients.


Your Ideal CDMO Partner for API Manufacturing

Pharmaoffer bridges the gap between pharmaceutical professionals and top CDMOs in the API sector. Whether it's for generic drugs or novel therapeutics, our listed CDMOs are equipped with the expertise and technology to support your API manufacturing needs, from small-scale lab production to large-scale commercial batches.