Apino Pharma Co., Ltd. - CDMO/CMO

Apino Pharma focuses on phamraceutical industry especially APIs and Key Intermediates as well as full service from R&D stage to commercial stage with the concept of “Added Value, Profession, Innovation”. We strictly follow the principle “Quality First” by supplying most reliable quality, professional service and reasonable price for the customers. Core product: peptide, Semaglutide, Tirzepatide, Retatrutide, Liraglutide, with approval of US FDA and EDQM.

Address: No.43 Cuijing Road, Zhukeng Community, Longtian Street, Pingshan District, Shenzhen, China, 518118, shenzhen
China

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Leading supplier for peptide, pharmaceutial raw material

Drug Substance

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Employees:

10+

Established in:

2019

Services

Drug Substance (CDMO/CRO)

Small molecule APIs form the backbone of many pharmaceutical drugs due to their low molecular weight and ease of synthesis. They are widely used in treating a range of diseases and are typically produced through chemical synthesis in GMP-compliant facilities.

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Contact Apino Pharma Co., Ltd. for Contract Services Expertise

Connect with Apino Pharma Co., Ltd., a leading pharmaceutical company from China. They offer specialized Drug Substance (CDMO/CRO). Contact Apino Pharma Co., Ltd. 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.