Our Services

R&D is our driving force for sustainable development. We own a mature and professional R&D team. In addition, high R&D budget for development of specialty generics which have high barriers or are difficult to replicate is allocated yearly.

Process of Product Development

Patent Evaluation

Patent evaluation is vital for drug development and launch. We have experienced patent assessors to do patent analysis and new patent application
Product Selection and development

We select an appropriate raw material and professional process design in order to meet the increasingly stringent requirements of the regulation. We focus on products which are challenging to make process such as oral disintegrating tablets, controlled released products, softgels and highly potent products. Currently we have several exclusive products in Taiwan.
Regulatory Affairs

We have very experienced regulatory affairs specialists who are familiar with CTD/ACTD dossier preparation and submission processes, and we have successful experiences on dossier submission to Taiwan, Japan, the U.S. and ASEAN countries.
R&D Team

We have over 10 years of experience in formulation design and bioequivalence relevant study. With the successful experiences, we are capable of practicing and controlling the progress of product development and tests in order to accelerate the procedures of registration. Currently we are certified to produce more than a hundred of pharmaceutical products.

Patent Evaluation

Patent evaluation is vital for drug development and launch. We have experienced patent assessors to do patent analysis and new patent application

Product Selection and development

We select an appropriate raw material and professional process design in order to meet the increasingly stringent requirements of the regulation. We focus on products which are challenging to make process such as oral disintegrating tablets, controlled released products, softgels and highly potent products. Currently we have several exclusive products in Taiwan.

Regulatory Affairs

We have very experienced regulatory affairs specialists who are familiar with CTD/ACTD dossier preparation and submission processes, and we have successful experiences on dossier submission to Taiwan, Japan, the U.S. and ASEAN countries.

R&D Team

We have over 10 years of experience in formulation design and bioequivalence relevant study. With the successful experiences, we are capable of practicing and controlling the progress of product development and tests in order to accelerate the procedures of registration. Currently we are certified to produce more than a hundred of pharmaceutical products.

R&D Blueprint

Control-released drugs development

e.g. Controlled-release medication and other special formulations
Products for Women related diseases

e.g.Endometriosis, Infertility……
High Barrier Generic Drugs

e.g. Softgels…
Highly potent drug development

e.g. Hormone based drugs, Oncology drugs.

Control-released drugs development

e.g. Controlled-release medication and other special formulations

Products for Women related diseases

e.g.Endometriosis, Infertility……

High Barrier Generic Drugs

e.g. Softgels…

Highly potent drug development

e.g. Hormone based drugs, Oncology drugs.

Contract manufacturing service

PeiLi’s Taiwan factory has passed GMP inspections by PMDA and TFDA. We are capable of offering contract manufacturing services not only for general medicines but also highly potent products, such as tablets, capsules, softgels, suppositories, ointments and granules.

Our Kunshan factory has passed China’s new GMP qualification in 2014. There are oral medicines and suppositories production lines to support China’s domestic market.

Contact us

CONTACT US

HEAD OFFICE

TEL：+886 4-23592576
FAX：+886 4-23590992
EMAIL：service@peili.com.tw
ADD：No. 11, Gongyequ 6th Rd., Xitun Dist., Taichung City 40755, Taiwan (R.O.C.)

KUNSHAN OFFICE

TEL：+86 512-5767274
FAX：+86 512-57874266
EMAIL：kunshan@peili.com.tw
ADD：No. 27, Lufen Road, Kunshan City, Jiangsu Province, China