CPC Scientific to Showcase Peptide and Oligonucleotide CDMO Leadership at CPHI Frankfurt 2025

Rocklin, CA – CPC Scientific Inc., a global Contract Development and Manufacturing Organization (CDMO) specializing in peptides and oligonucleotides, and a subsidiary of Medtide Inc., will have a major presence at CPHI Frankfurt 2025, taking place October 28–30 at Messe Frankfurt, Germany.

As its flagship annual event, CPC Scientific will spotlight its leadership in the rapidly expanding peptide and oligonucleotide sector and its strategic role as a trusted global partner.

Driving Innovation in Peptides and Oligonucleotides

CPC Scientific is well-positioned to capture emerging opportunities in the growing global TIDES drug market, especially in the dynamic GLP-1 therapeutic space. Visitors can connect with CPC Scientific at Booth 12.0F29 (Hall 12, API Zone), where the company will present its end-to-end CRDMO services supporting every stage of drug development, from discovery, clinical development to large-scale commercial supply.

Strong team presence

As part of its global engagement strategy, CPC Scientific will bring together leadership, business development, and scientific expertise to CPHI, including:

• Shawn Lee, Founder & CEO
• Theresa Cheng, President
• Tim Nieters, Senior Vice President of Strategic Portfolio Development
• Joseph Denby, Senior Business Development Manager
• Clàudia Badia i Lopez, Business Development Manager
• James Gao, International Business Manager

The team will connect with existing and prospective partners to reinforce collaborations, explore new opportunities, and demonstrate the company’s enhanced capabilities and expanded capacity.

To book a meeting, email [email protected] or visit https://cpcscientific.com/event/cphi-frankfurt/.

Well-Positioned for Growth

CPC Scientific has adopted a “going with the compound” strategy, aligning capacity with customer demand and industry trends. Many projects in the pipeline are expected to enter commercial production in the next three to five years, driven by:

• Anticipated commercialization of multiple peptide programs
• Rapid global demand for peptide drugs, especially GLP-1 and obesity products
• Rising opportunities in generics as key patents expire across major markets

CRDMO strengths

CPC Scientific delivers industry-leading CRDMO services with consistent advantages in quality, efficiency, and scalability:

• Comprehensive Capabilities: CPC Scientific provides complete lifecycle support, from discovery and preclinical research through Phase I–III clinical development to commercial manufacturing. Its integrated model minimizes hand-offs and risk, ensuring seamless execution.
• Regulatory excellence: Backed by nearly 25 years of expertise and a >99.95% new-molecule synthesis success rate. CPC Scientific has successfully passed 5 FDA on-site GMP inspections and 3 additional inspections by the EMA, MFDS, and TGA. In the past five years alone, the company has also completed 9 NMPA on-site or registration inspections. Certified to ISO 9001 and ISO 13485 standards.
• Scale and innovation: Cutting-edge peptide production technologies and metric-ton scale GMP API capacity deliver unmatched efficiency and competitive scalability, with annual peptide API production of over 1,000 kg.
• Trusted worldwide: Proven track record of strong, long-term partnerships with leading pharmaceutical and biotech companies across 50+ countries, supporting both NCEs and generic peptide development.
• GLP-1 expertise: A recognized leader in oral and injectable GLP-1 and obesity programs, one of the most dynamic and fastest-growing segments of the global peptide drug market.

About CPC Scientific, Inc.

With nearly 25 years of experience, CPC Scientific is a globally recognized Contract Research, Development, and Manufacturing Organization (CRDMO) that specializes in synthetic GMP peptides, oligonucleotides, and peptide-oligonucleotide conjugates (POCs), while offering a full range of research-grade custom and catalog products. Our integrated service model is designed to support partners through the most critical phases of drug development, with a particular focus on late-phase development, large-scale manufacturing, and commercial production. From initial discovery to full commercialization, we provide the expertise and robust infrastructure to accelerate peptide and oligonucleotide programs to success, backed by metric-ton scale GMP manufacturing and an annual production capacity exceeding 1,000 kg.

CPC Scientific meticulously follows FDA and ICH guidelines for CGMP manufacturing, and we provide complete support for your IND, NDA, and BLA filings in the USA and all international filings and required regulatory support for your active pharmaceutical ingredients (APIs). Our New Chemical Entity (NCE) development program involves process development, process validation, analytical method development, method validation, stability studies, regulatory support, and assistance preparing regulatory documents. We also have flexibility, pre-qualified workspace, and robust supply chain to incorporate new projects into our pipeline rapidly. We understand that delivery time is critical to your project’s success, and we have the capacity and flexibility to accept new projects and initiate production sooner than many leading CDMOs.

With a USA facility in Rocklin, near Sacramento, California, CPC Scientific is a subsidiary of Medtide Inc., which officially listed on the main board of the Hong Kong Stock Exchange in 2025.

Learn more at: https://cpcscientific.com

Resources

Click on CPHI Frankfurt 2025 for further event information and registration.
Click on CPC Scientific News and Articles to see latest News & Events.