CDMO Services
the right cdmo partner for youCDMO Services
Prestige Biologics provides CDMO services that support the entire lifecycle of biopharmaceutical products, from development through commercial manufacturing.
Tailored solutions are designed to meet the specific characteristics and development stage of each product, enabling efficient and reliable project execution through extensive technical expertise and manufacturing capabilities. Through continuous process innovation and advancements in bioprocessing technologies, Prestige Biologics supports accelerated development timelines and successful product commercialization while establishing a robust manufacturing environment capable of ensuring a stable and timely supply of biopharmaceutical products.
One-Stop Solution
Prestige Biologics is committed to supporting the success of each customer’s pipeline.
Integrated support is provided across the full drug development lifecycle, including technology research, process development, clinical manufacturing, commercial manufacturing, clinical support, and IND and BLA filing. Through these capabilities, Prestige Biologics delivers effective solutions tailored to customer needs in the rapidly evolving biopharmaceutical market.
Prestige Biologics strives to be a dedicated partner, combining its experience and technology with a shared commitment to each customer’s success.
Features
What We Service
PROCESS DEVELOPMENT
ENGINEERING
CLINICAL MANUFACTURING & SUPPORT
QUALITY MANAGEMENT
IND & EMA MAA
COMMERCIAL PRODUCTION
4-Week CDMO Quotation Program
Prestige Biologics provides preliminary quotation services for clinical and commercial manufacturing projects across various development stages, from early- to late-stage programs. Within four weeks, customers can review estimated manufacturing costs and technical strategies for each development phase, enabling the establishment of a manufacturing strategy that extends through commercial production.
3-Week CPO Quotation Program
Prestige Biologics provides secondary packaging services tailored to customer requirements, with packaging operations performed at GMP-certified facilities in compliance with EU and international GMP standards. Project-specific SOPs are established and implemented in accordance with GMP requirements, based on each customer’s defined specifications.
Analytical Testing Service Quotation Program
Prestige Biologics provides a wide range of analytical services tailored to customer needs, from routine analytical testing to analytical method development and validation. Analytical method development and testing services tailored to the specific characteristics of each pharmaceutical product are performed by experienced analytical scientists using advanced equipment, helping customers reduce both time and cost.
Open Door Policy for Customers
Prestige Biologics operates an Open-door Policy founded on transparent information sharing and close collaboration to deliver customer-centric services. We proactively communicate key project updates and critical issues throughout the development and manufacturing lifecycle, enabling rapid decision-making and efficient problem resolution through seamless communication.
Through continuous engagement and collaboration with our customers, we support the successful execution of projects and the achievement of project objectives while fostering long-term partnerships built on trust and mutual success.
Guided by our corporate philosophy, “Innovation for Life,” Prestige Biologics contributes to the development and manufacturing of biopharmaceuticals that improve patients’ lives through open collaboration, innovation, and sustainable growth.
