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ChemCon GmbH - CDMO/CMO
At ChemCon GmbH, we specialize in the complete development and transfer of chemical processes, ensuring seamless scalability from R&D to GMP production. With exceptional expertise in both production and analytical services, we provide tailored solutions for our customers’ most challenging needs, from early clinical trials to commercial production.
Specialized Expertise:
- Isotopically Labeled Compounds & Cold Precursors:
- Tailored solutions for research and development applications.
- Cytotoxic and Highly Potent Substances (HPAPIs):
- Safe and reliable handling of HPAPIs and controlled substances.
- Diverse Chemical Disciplines:
- Expertise in organic,...
Germany
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Exceptional Regulatory Support: We guide you from the first clinical trials through to the commercial phase, ensuring compliance and efficiency every step of the way.
Production Flexibility: From initial process development at scales as low as 0.5 g to commercial manufacturing for both small and larger demands.
Integrated Analytical Services: In-house method development, validation, and comprehensive release analytics tailored to your needs.
Our services:
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Services
Our Core Services:
- Route of Synthesis Development:
- Comprehensive development of synthetic pathways.
- Route scouting and process optimization for efficiency and scalability.
- Process Improvement & Customer Collaboration:
- Optimization of processes provided by customers.
- Scale-up of customer processes, including development and execution of GMP synthesis.
- Analytics Development & Validation:
- Creation and in-house validation of analytical methods for robust quality assurance.
- Development of necessary release analytics to meet regulatory standards.
- Literature Research &...
Drug Substance (CDMO/CRO)
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Contact ChemCon GmbH for Contract Services Expertise
Connect with ChemCon GmbH, a leading pharmaceutical company from Germany. They offer specialized Drug Substance (CDMO/CRO). Contact ChemCon GmbH for free and discover if they are the perfect partner for your pharmaceutical needs.
Drug Substance (CDMO/CRO)
Drug Substance CDMOs and CROs provide essential services in the development and manufacturing of active pharmaceutical ingredients (APIs). These organizations specialize in early-stage research, process development, and GMP-compliant manufacturing of drug substances for clinical and commercial use.
Pharmaoffer's Drug Substance CDMO/CRO category includes partners with expertise in small molecules, biologics, peptides, and complex chemistry, all operating under strict regulatory compliance. These providers help companies scale from lab to market efficiently and cost-effectively.
Key Functions of Drug Substance CDMOs/CROs:
API Research and Development: Providing early-stage discovery support, custom synthesis, and process optimization to streamline the development of drug substances.
Process Scale-Up and Tech Transfer: Transitioning from bench-scale to pilot and commercial scale production with validated methods and reproducibility.
GMP Manufacturing: Delivering high-quality API batches in GMP-certified environments, adhering to FDA, EMA, and other international standards.
Analytical Services: Offering comprehensive analytical method development and validation to ensure consistent quality and regulatory compliance.
Flexible and Specialized Capabilities: From small molecule synthesis to biologic and peptide manufacturing, these partners provide specialized services tailored to product-specific needs.
Explore Leading API CDMOs and CROs
Pharmaoffer connects you with trusted CDMOs and CROs for drug substance development. Our platform enables seamless access to specialized service providers equipped to support your API lifecycle from discovery to commercialization.