ABOUT USOur Journey

We are a pre-eminent full-service contract manufacturer, packager and formulation expert of superior quality tablet, capsule, powder, and liquid natural health products for the Canadian, U.S., and international markets.
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Before 1996

BEFORE 1996

High-Performance Liquid Chromatography

Dr. Ma and his team developed multiple High-Performance Liquid Chromatography (HPLC) methods in UK and Canada.

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1996

MARCH 1996

Canadian Phytopharmaceuticals Corporation

As a founder, Dr. Ma established Canadian Phytopharmaceuticals Corporation (CPC) in British Columbia, Canada. Prior to CPC’s establishment, Dr. Ma proposed the ginsenoside content ratio in the ginseng plant. This allowed for future HPLC profile development for Panax species. The results have been recognized as international standards.

LATE 1996

Standardization

Dr. Ma actively promoted the concept of Standardization in botanical medicines.

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1997

FALL 1997

Pharmaceutical Analysis

Dr. Ma, as a player in pharmaceutical analysis, participated in the ginseng evaluation program closely working with American botanical council.

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2001

EARLY 2001

First International Conference

Dr. Ma collaborated with the Chinese State Drug Administration to organize the first International Conference on the Standardization of Phytopharmaceutical Products in Beijing, China.

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2004-2005

2004 TO 2005

Good Manufacturing Practice

Good Manufacturing Practice (GMP) required by Health Canada, all manufacturers in Canada must meet the requirements.

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2005

EARLY 2005

National Research Council of Canada

Dr. Ma signed the contract with the National Research Council of Canada for the research project on Goldenseal. He and his team focused researching on the analysis of formulated botanical products. He specifically focused on the analysis of multiple chemical constituents.

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2005

EARLY 2005

National Research Council of Canada

Dr. Ma signed the contract with the National Research Council of Canada for the research project on Goldenseal. He and his team focused researching on the analysis of formulated botanical products. He specifically focused on the analysis of multiple chemical constituents.

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2006-2008

2006 TO 2008

The Stability Testing

Dr. Ma and his team started working on the stability testing for Natural Health products which pushed the industry for Natural Health product to a higher level.

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2009

2009

RRLC Methods

Dr. Ma and his team utilized RRLC methods to analyze most popular botanical extracts and finished products such as Rhodiola, Epimedium and different ginseng species.

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2010-2015

LATE 2010 TO 2015

Scientific Research Papers

A series of scientific research papers were published by Dr. Ma and his research team on the formulated botanical products.

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2015-2018

2015 TO 2018

The United States Pharmacopoeia

Dr. Ma and his team’s research work on the analysis of Rhodiola, Reish mushroom, Panax notoginseng, Ginkgo biloba, have been accepted by the United States Pharmacopoeia as monographs and international standards.

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