A TECHNO-ECONOMIC NEWS MAGAZINE FOR MEDICAL PLASTICS AND PHARMACEUTICAL INDUSTRY
Our 15th Year of Publication
Page  2 of 8

Cover Story

Invited Speakers : Abstracts & Introduction

 

Polymedicure Pvt. Ltd.

Mr. Himanshu Baid,
Director
Polymedicure Pvt. Ltd.

About Speaker

Background of how Polymed was conceived under guidance of Sh. J.K.Baid.

Model role played by Mr. D.L.Pandya in selecting the products, technology & Market feasibility report.

Abstract

 

Focus areas for developing business were (1) investment in R&D (2) work mainly with companies who have prior experience of manufacturing Medical Devices (3) sell quality products in developed & regulated markets (4) To invest in Internal & External Training (5) To set up an effective Information Management & governance system (6) set up KRA/KPI’s at all levels in the organization 7) Empower employees so that decision making becomes fast at all levels (8) Rely on Innovation as the only engine for future success. (9) To put a strategy in place and achieve Apex goals like Brand Leadership, Business Volume & Internal Excellence.


Size of Indian Medical Device Industry which includes complex products such as drug eluting stunts, implants, pace makers to Syringes, Needles etc is approx Rs.4000 Crores.


80% of the Medical Devices are imported into India. Indian Medical Devices Industry has not invested enough in R&D to develop new products & is mostly relying on mee-too products.


On the contrary China has over 15000 manufacturers of Medical Devices and size of the industry is approx 16000 crores. Most of the outsourcing done by USA & European companies is done in China. Due to increasing costs in the west as per Industry estimates there is a possibility of US$ 10 Billion outsourcing opportunity into low cost manufacturing countries including India, China & Vietnam etc. in next 10 years.


As per the current scenario most of the Indian medical Devices companies were unregulated and due to this the standard of manufacturing was not up to the Global acceptable requirements. The need of the hour is to regulate the Industries as per EU Medical Device Regulation (MDD) or follow GHTF (Global Harmonized Task Force) guidelines to bring Indian Medical Device Companies at par with International Standards.


Jointly we can all create Training programs for all stake holders i.e users, Industry & regulators & Participate in GHTF, AHWP & other global initiatives to bring Indian companies to Global standards..

 

Dr. S. P. Adesara Former Commissioner, FDCA (Gujarat State)

About Speaker

 

Dr Adesara has been actively involved in the process of Regulatory Reforms for Indian Medical Device Industry by Ministry Of Health & Family Welfare , Govt. of India. Being the head of FDCA in Gujarat State, which has more than 30 % contribution in the production of Pharmaceuticals and Medical Devices in India , his role has been prominent in implementation of the Regulatory Reforms while at the same time mentoring Indian Medical Device Industry for facing the challenges of reforms.

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