- Synthetic circuit design and screening
- Process reference and quality attributes are accurate
- Process safety risk assessment
- Analytical method development and improvement
- Journal spectra confirm and toxic impurities
- Preparation, analysis and calibration of analytical controls
- The formulation of quality standards
- Glass kettle or pilot kilogram production
- Stability investigation
- Preparation and filing of registration documents for INDs
CDMO services
Drug screening (SAR), preclinical research (CMC), clinical sample box registration support, peptide API supply
Scientific research Customized peptides
R&D processes ranging from grams to kilograms/from simple to complex
Peptide
SERVICES
CRO services
Scientific research customized peptide synthesis services
PDC Drug Synthesis Services
ADC Linker Drug Synthesis Services
FFS/FTE management services
CDMO services
MTDrug-CDMO
MTCosme-CDMO
CMO services
GMP
Personalized services for tumor antigen peptides
Testing services
Testing services
CRO
Early research
Dr discovery
Preclinical research
CDMO
Preclinical
Clinical phase I
Clinical stage II
Clinical stage III
Clinical phase services
- Continuous process improvement and optimization
- Quality Risk Analysis (QRA) based on QbD concept
- Material quality studies: analytical method development, validation and quality standard development
- Intermediate product quality research: analytical method development, verification and quality standard formulation, stability research
- Product quality research: further improve impurity research, further improve analysis methods and quality standards, and stability investigation
- Initiating the transfer of raw materials to API analysis methods
- API production process transfer
Commercialization
New drug registration and cGMP commercial production under the MAH regime
- Registered batch starting material inspection, registered batch intermediates and API cGMP production
- Continuous process improvement and commercial production
- Continuous stability inspection
- Process validation for NDA declarations
- NDA registration document writing and filing
Peptide
PRODUCTS
Peptide drug impurities
Semaglutide full set of impurities
A full set of impurities for tirpotide
Retaglutide full set of impurities
Customized peptide impurities
Peptide drug APIs/intermediates
Disease
Endocrine and metabolic regulation
Cardiovascular system regulation
Immune system
Regulation and protection of physiological functions
Beauty peptides
Anti-aging
Repair
Whitening
Moisturizing
Body care
Anti-inflammatory
Popular peptide products
Linker
Adrenocorticotropic hormone
Angiotensin
About us
ABOUT US
35+years
Industry cooperation experience
1000+
Cooperative customers
2
Production base
Suzhou Murdiff Biotechnology Co., Ltd. is an innovative peptide biotechnology company specializing in the customization, research and development, production and service of peptide-related products. With peptide technology as the core, the company is committed to developing into an international peptide CRDMO enterprise integrating peptide scientific research and customization, peptide drug research and development, peptide drug process development, and peptide API production.
News
NEWS CENTER
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How can we help you?
HOW CAN WE HELP YOU?
Technical advantages
(1) Rich experience in peptide customization
Serving more than 1500+ customers with peptide customization needs, it can ensure the maintenance of amino acid configuration and the reduction of by-products during peptide synthesis, so that peptides have the best biological activity.
(2) Precise control of peptide synthesis difficulties
It can accurately control the difficulty of partial removal, the selection of glycosylation sites, the coupling site and the degree of modification, and add reaction process monitoring to the stapling peptide ring process.
Production capacity
The GMP production workshop designed and built in strict accordance with the guidelines and specifications of ICHQ7 can produce peptide raw materials of different scales, and the service content mainly includes three aspects: customized development services, GMP standard small test and pilot test, and GMP scale-up production. Yields range from milligrams to kilograms.
GMP production workshop water treatment system, air circulation system, production and inspection equipment have passed 3Q verification. In terms of production equipment, it is equipped with large-scale solid-phase synthesis 5L, 10L, 20L, 30L, 50L reaction equipment and liquid phase reaction equipment (peptide synthesis)......
One-stop service
(1) Scientific research customized peptide service platform
Long-term peptide modification and optimization service platform
(2) MTCosme beauty peptide one-stop service platform
In the research and development of new beauty peptide raw materials, Merdiff has an experienced R&D team to make innovative proportional schemes for the efficacy of new raw materials......
(3) MTDrug-CDMO one-stop service platform
Available to peptide drug researchers worldwide, including chain/ring ......