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Drug Substance (CDMO/CRO) - CDMO/CMO
Founded in March 2011, Apollo Healthcare Resources is the most comprehensive distributor of Active Pharma Ingredient (API) and Excipient in Singapore. Carry over 1000 products to cater the needs of industries of Pharmaceutical, Personal Care, and Food & Beverage, we serve clients across 61 countries.
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In this edition of eBulletin, we share the experience of pharmaceutical industry expert Apollo Healthcare Resources (AHR) – a Singapore SME ready for its own advancement with the strategic optim
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Founded in March 2011, Apollo Healthcare Resources is the most comprehensive distributor of Active Pharma Ingredient (API) and Excipient in Singapore. Carry over 1000 products to cater the needs of industries of Pharmaceutical, Personal Care, and Food & Beverage, we serve clients across 61 countries.
YOUR MATERIALS, OUR EXPERTISE!
Drug Substance (CDMO/CRO)
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Contact Drug Substance (CDMO/CRO) for Contract Services Expertise
Connect with Drug Substance (CDMO/CRO), a leading pharmaceutical company from Singapore. They offer specialized Drug Substance (CDMO/CRO). Contact Drug Substance (CDMO/CRO) 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.