Active Pharmaceutical Ingredients for development and manufacturing.

High-quality APIs, with access to R&D, manufacturing and regulatory documentation support in China.

Explore products
ProductsAPIs, intermediates and excipients
R&D supportProcess and analytical method development
Production capabilityPilot, scale-up and commercial manufacturing
RegulatoryDocumentation and cGMP audit support

Products

Our portfolio covers a wide range of therapeutic categories.

Company Overview

Sijia Pharm is a China-based supplier of APIs, advanced intermediates, excipients, and reference standards. We provide strong regulatory support (DMF / ASMF / CEP) and accompany clients from development to commercial supply with technical expertise and reliable service.

01
ShenzhenSijia Pharm office

Product supply and coordination

02
WuhanR&D centre

3,000 m² · 90 employees · more than 60 R&D personnel for novel products (CRO/CDMO)

03
JingmenProduction site

5,000 m² · 30+ reactors · 112,700 L total volume

ShenzhenSijia Pharm office

Product supply and coordination

R&D Centre

A 3,000 m² centre supporting customised production of intermediates and APIs from gram to ton, novel product process development and optimisation, and multi-variety inventory reserves.

90 employees25% with PhD and Master degree
More than 60R&D personnel
20 / 50 / 100 Lglass reactors
−78 to 200 °Creaction range

Analytical equipment

HPLC, GC, Karl Fischer moisture analysis, potentiometric titration, stability study and LCMS.

Process capabilities

Asymmetric catalytic reduction, metal-coupling reactions, low-temperature butyllithium reactions and amination.

Production Site

A 5,000 m² multi-purpose modular workshop supporting flexible scale-up and commercial production of pharmaceutical intermediates and APIs.

5,000 m²multi-purpose workshop
30+ reactorsseven working volumes
112,700 Ltotal reactor volume
−100 to 250 °Creaction range

Reactor configuration

500, 1,000, 2,000, 3,000, 4,000, 5,000 and 6,300 L reactors in glass-lined steel, stainless steel and Hastelloy.

Specific processes

Hydrogenation up to 10 MPa, chlorination, fluorination, amination and ultra-low-temperature reactions.

EDQM
USP
cGMP

Quality & Regulatory

EP, USP, CP and in-house standards.

DocumentationDMF in CTD format / ASMF / CEP
Audit supportcGMP audit support

Contact

Start a direct conversation.

Email the sales team
Shenzhen Sijia Pharmaceutical Co., Ltd.
Telephone+86 755 8665 5580
Shenzhen officeRoom 610, Tower A, One Excellence Qianhai, No. 5033 Menghai Blvd., Nanshan District, 518052, Shenzhen City, China