The GMP model research of Hechuan Biopharmaceutical meets the NMPA, FDA, and EMA review requirements

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The GMP model research of Hechuan Biopharmaceutical meets the NMPA, FDA, and EMA review requirements

$negotiable / kilogram

Reference Price

1kilogram (Min. Order)

Ship From

Suzhou, Jiangsu

Shipping

To be negotiated with the supplier

Customization

For customization requests, please

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Hechuan professional testing instrument GC-MS LC-MS NMR HPLC comprehensive analysis

Brand

Hechuan

Medicine+

Conduct project research according to GMP mode

Market scope

China, United States, European Union, etc

Synthesis process

To be determined

Analysis of Pharmaceutical Ingredients

provide

Service Type

Consulting/Planning

Report Type

Reports that comply with regulatory requirements in China, the United States, the European Union, and other countries

Formulation development stage

Effective ingredient content detection

Project research mode

Follow GMP mode

Recognized by industry associations

Yes

Quality improvement

change the world

Smooth stability

Drug solubility test, drug stability test

Custom packaging materials

Compatibility research plan

System Solution

Composition analysis, quality control plan, etc

analytical method

Physical and chemical constants, identification tests, various detections, etc

Raw materials and additives

Source control

research methods

Market research

Review requirements

Meet the review requirements of NMPA, FDA, and EMA

Patent scheme

A large number of authorities

After-sales guarantee

Perfect

Ten years of analytical experience

have

Application of analytical techniques

System Solution

Company founding date

2012

expert team

Professional

Details

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