Cellipont Bioservices - CDMO/CMO

Cellipont Bioservices is a key player in the CDMO landscape, with a specific focus on cell and gene therapy products. They offer comprehensive services from process development to commercial manufacturing, with a particular expertise in autologous and allogeneic cellular therapies. Their facilities are designed to meet the complex needs of cell-based therapies, ensuring adherence to stringent regulatory standards.

Address: 9501 Lakeside Blvd., TX 77381, The Woodlands
United States

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Expertise in cell therapy development and manufacturing.

Tailored solutions for autologous and allogeneic cell therapies.

Cutting-edge technology for scalable and efficient cell therapy production.

Drug Substance

Drug Product

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Drug Substance (CDMO/CRO)

Cell and gene therapy (DS)

CDMOs for cell and gene therapy drug substances offer capabilities in cell banking, viral vector production, upstream/downstream processing, and analytical support for ATMPs.

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Drug Product (CMO)

Cell and gene therapy (DP)

Cell and gene therapy drug products require highly specialized handling and aseptic manufacturing. CDMOs offer end-to-end support from final formulation to commercial-scale fill-finish.

Replies slower than most

Contact Cellipont Bioservices for Contract Services Expertise

Connect with Cellipont Bioservices, a leading pharmaceutical company from United States. They offer specialized Drug Substance (CDMO/CRO), Drug Product (CMO). Contact Cellipont Bioservices 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.

Drug Product (CMO)

Drug Product CMOs focus on the manufacturing and packaging of finished pharmaceutical dosage forms. These contract partners provide scalable production solutions that meet global regulatory and quality standards, supporting pharma companies throughout the drug product lifecycle.

Pharmaoffer’s Drug Product CMO category includes providers capable of manufacturing oral solids, injectables, topical formulations, and more—whether for clinical trials or commercial distribution.

Key Functions of Drug Product CMOs:

Formulation Development: Supporting the transition from drug substance to drug product through formulation optimization and compatibility testing.
Clinical and Commercial Manufacturing: Offering pilot-scale to high-volume manufacturing for various dosage forms under GMP conditions.
Packaging and Serialization: Providing primary and secondary packaging with serialization and tamper-proof labeling to meet compliance requirements.
Regulatory Support: Ensuring that all production meets FDA, EMA, and ICH standards for drug product quality, safety, and traceability.
Flexible Production Lines: Handling diverse dosage forms including tablets, softgels, liquids, and sterile injectables.

Partner with Proven Drug Product CMOs

Through Pharmaoffer, discover CMOs that excel in drug product manufacturing. Whether you need small-scale batches or full commercial output, our platform connects you with the right partners for compliant, cost-effective solutions.