CN
CDMO SERVICE
15 Years of Excellent Service in Pre-formulation and Formulation
Polymorph and Crystallization Topical & Transdermal Delivery Complex Generics Accelerated FIH Development GMP Manufacturing Analytical Testing
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CDMO SERVICE
Excellent Service in Pre-formulation and Formulation

SoliPharma excels in solid-state research and complex formulation. As a leading CDMO, we provide comprehensive development and manufacturing services to global clients. By harnessing our expertise, we maximize the potential of your innovative drug molecules.

SoliPharma has been a trusted CDMO partner for over 15 years, serving 800+ global clients. We've successfully completed pre-formulation and formulation for 2000+ compounds at different clinical stages and annually generated 200K+ analytical testing reports, empowering our clients to navigate IND/NDA/ANDA submissions with confidence to both China NMPA and US FDA.


800+
CXO Clients
2000+
Projects Completed
20000+
Annual Testing
100+
Formulation Cooperation
SoliTech® Innovation Institute is a nationally accredited innovation hub. The institute concentrates on topical and transdermal drug delivery, delving deep into the design and control of micro-delivery systems. The institute is organized into four centers: Polymorph & Crystallization, Topical and Transdermal Drug Delivery, Complex Generics, and Accelerated FIH Development.
This laboratory is accredited as National-level Postdoctoral Research Workstation, Provincial Research Institute for Topical and Transdermal Drugs, and Provincial Research Center for Highly Variable Drugs.

●   Form Screening and Crystallization Development

 

●   Control of Solid Form in Finished Products

 

●   Crystal Growth of Polymeric Additives

●  Formulation Development for Poorly Soluble Drugs

 

●  Formulation Development for Poorly Permeable Drugs

 

●  Formulation Development for Reactive Molecules


●  Development of New Permeation Enhancer

 

● Follicular Target Delivery

 

● Extended Release for Topicals


●  Semi-Solids

 

●  Fixed Dose Combination

 

●  Formulation with Complex APIs


Polymorph & Crystallization
Accelerated FIH Development
Topic and Transdermal Drug Delivery
Complex Generics
OUR SERVICE
Polymorph and Crystallization

Form Screening & Selection , Crystallization Process Development , Form Control in Drug Product


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Topical & Transdermal Delivery

Innovative Technologies for Enhanced Penetration , Follicular Target Drug Delivery , Extended Release of Topical and Transdermal Delivery


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Accelerated FIH Development

FIH Development Accelerator

Regulatory Filing to Multiple Authority Agencies

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Complex Generics

Complex formulation including:Topical (gel, cream, ointment, emulgel, solution etc.)


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GMP Manufacturing

Multiple Dosage Forms

Flexible batch size

Pass NMPA & FDA GMP Inspection 


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Analytical Testing

Comprehensive Analytical Testing , Method Development and Validation , Conforms to GMP/CNAS/UL


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OUR STRENGTH
Technical Strength
Facility Strength
Service Strength

●  Our team’s state-of-the-art material characterization capabilities deliver reliable results and accelerate drug development.


●  Our GMP facility features multiple production lines and versatile equipment size to accommodate diverse batch demands for clinical or commercial supply.

 

●  We have successfully passed GMP inspections from prestigious organizations including USFDA, NMPA, and UL, and we have also obtained CNAS accreditation.


●  We have provided more than 15 years of excellent service to the pharmaceutical industries.

 

●  Our in-house R&D experience database features a diverse collection of over 200 formulation protocols and more than 20 animal models.

 

●  Our services have extended to over 800 global clients, and have conducted pre-formulation and formulation development for more than 2,000 molecules across different clinical phases.