14
AFFORDABLE, CREDIBLE, EFFICIENT RESEARCH Preclinical, Safety and Quality Standardization Studies for Nutraceuticals

Preclinical, safety and quality standardization studies for nutraceuticals

Embed Size (px)

DESCRIPTION

 

Citation preview

Page 1: Preclinical, safety and quality standardization studies for nutraceuticals

AFFORDABLE, CREDIBLE, EFFICIENT RESEARCH

Preclinical, Safety and Quality Standardization Studies for Nutraceuticals

Page 2: Preclinical, safety and quality standardization studies for nutraceuticals

Vedic. Introduction

A decade of experience as full and functional service CRO Widest range of services for the Dietary Supplements,

Nutraceuticals, Botanical Drug Products, Medical Foods, Natural Health Products, Cosmetics & Personal Care Products

Clinical & Preclinical studies for label claim substantiation Compliant data to meet regulatory requirements Studies to check compliance with Dietary Supplement cGMP ISO 9001:2008 certified

2

Page 3: Preclinical, safety and quality standardization studies for nutraceuticals

Vedic. Services3

Page 4: Preclinical, safety and quality standardization studies for nutraceuticals

Vedic. Preclinical

Pharmacological Screening studies - in vitro and in vivo Toxicology and Safety studies Bioavailability studies for active ingredients and finished

products Analytical Development Formulation Development Completed 300+ studies (GLP and Non GLP) Drug Interaction Studies

4

Page 5: Preclinical, safety and quality standardization studies for nutraceuticals

Vedic. Pre Clinical5

Page 6: Preclinical, safety and quality standardization studies for nutraceuticals

Vedic. Toxicology

6

6

Page 7: Preclinical, safety and quality standardization studies for nutraceuticals

Vedic. Preclinical Claim substantiation (Animal Pharmacology)

Professionally drafted Protocols Numerous In vitro and In vivo models available Investigators with experience in specific fields Well maintained animal houses Close monitoring Authentic data ensuring audit trail Speedy data analysis, reporting, paper writing Co-ordination of multi-site projects

7

Page 8: Preclinical, safety and quality standardization studies for nutraceuticals

Vedic. Analytical Method Development & Validation

Protocol Development as per International Standards Analytical Method Development. Measurement of Markers/Biomarkers for Research, Nutraceutical

Products Development, using HPLC or LC/MSMS Validation of methods to FDA/EMEA (EFSA ?)guidelines in

accordance with GLP/GCP regulations

8

Page 9: Preclinical, safety and quality standardization studies for nutraceuticals

Vedic. Formulation Development

9

9

Page 10: Preclinical, safety and quality standardization studies for nutraceuticals

Vedic. Partners

Product Formulation Facility

Microbiology Laboratory

Test Item Control Unit

10

Page 11: Preclinical, safety and quality standardization studies for nutraceuticals

Vedic. Key people

Jayesh Chaudhary is Founder & Managing Director of Vedic Lifesciences. He has been involved in product development and international business since 1994. He is thorough with regulatory affairs, research and marketing for nutraceutical and phyto-pharmaceutical actives and formulations for the EU and US markets. Trained in Pharmacy and Microbial Engineering from University of Minnesota, Jayesh was responsible for the Biocatalyst and Natural Products technical support and national sales at Boehringer Mannheim India in the early ‘90s.

Jayesh Chaudhary is Founder & Managing Director of Vedic Lifesciences. He has been involved in product development and international business since 1994. He is thorough with regulatory affairs, research and marketing for nutraceutical and phyto-pharmaceutical actives and formulations for the EU and US markets. Trained in Pharmacy and Microbial Engineering from University of Minnesota, Jayesh was responsible for the Biocatalyst and Natural Products technical support and national sales at Boehringer Mannheim India in the early ‘90s. • Dr. Navneet Sonawane is heading the Clinical Research

Department. She has 12 years of experience in the field of Medical Science & Clinical Research, which include areas such as Medical Writing, Regulatory Affairs, Project Management & QA. She has successfully headed Global Clinical Studies across various therapeutic segments. During her tenure at Vedic, she has developed a strong network of GCP trained clinical investigators around India and has been appreciated by Sponsors around globe. She places a high premium for meeting time line while ensuring delivering of quality.

• Dr. Navneet Sonawane is heading the Clinical Research Department. She has 12 years of experience in the field of Medical Science & Clinical Research, which include areas such as Medical Writing, Regulatory Affairs, Project Management & QA. She has successfully headed Global Clinical Studies across various therapeutic segments. During her tenure at Vedic, she has developed a strong network of GCP trained clinical investigators around India and has been appreciated by Sponsors around globe. She places a high premium for meeting time line while ensuring delivering of quality.

11

Page 12: Preclinical, safety and quality standardization studies for nutraceuticals

Vedic. Key people

Kunal Bhatt has 8 years of experience within the pharmaceutical industry, having led

several Global Phase I - IV drug studies in various capacities and diverse therapeutic areas

like Neurology, Psychiatry (Adult and Pediatric), Oncology, Diabetes, Urology and Cardiology.

Masters in Pharmacology and Biotech from Sheffield Hallem University, UK, Kunal has worked

in areas of Global Project Management, Clinical Operations and Regulatory. As a Global

Business Development Manager his good business planning acumen and interpersonal relations

help in crafting Business & Marketing Plans.

Kunal Bhatt has 8 years of experience within the pharmaceutical industry, having led

several Global Phase I - IV drug studies in various capacities and diverse therapeutic areas

like Neurology, Psychiatry (Adult and Pediatric), Oncology, Diabetes, Urology and Cardiology.

Masters in Pharmacology and Biotech from Sheffield Hallem University, UK, Kunal has worked

in areas of Global Project Management, Clinical Operations and Regulatory. As a Global

Business Development Manager his good business planning acumen and interpersonal relations

help in crafting Business & Marketing Plans.

Dr. Vijay Gokarn has 7yrs of experience in herbal & pharmaceutical research industry. Proficient in analytical method development & validation with proven expertise for standardization of single & multiherb preparations & preclinical bioassays. A PhD degree in Analytical Chemistry on Standardization of Botanicals from the University of Mumbai, he heads the Preclinical- Technical Department as Asst. Project Manager- Technical. Dr. Gokarn supports the group in advanced scientific standardization, validation & process development services in the field of Phytomedicine, Nutraceuticals & Ayurvedic preparations. 

Dr. Vijay Gokarn has 7yrs of experience in herbal & pharmaceutical research industry. Proficient in analytical method development & validation with proven expertise for standardization of single & multiherb preparations & preclinical bioassays. A PhD degree in Analytical Chemistry on Standardization of Botanicals from the University of Mumbai, he heads the Preclinical- Technical Department as Asst. Project Manager- Technical. Dr. Gokarn supports the group in advanced scientific standardization, validation & process development services in the field of Phytomedicine, Nutraceuticals & Ayurvedic preparations. 

12

Page 13: Preclinical, safety and quality standardization studies for nutraceuticals

Vedic. Social Media13

Page 14: Preclinical, safety and quality standardization studies for nutraceuticals

India 203, Morya Landmark 1, Off new Link Road, Andheri West,

Mumbai 400053

Tel.: +91 22 42172300 / +91 22 42025719

USA552, Shorebird Circle, Unit #1101, Redwood Shores, CA.

94065

Tel.: (650) 855-4832

[email protected], www.vediclifesciences.com

14