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Panel of Experts
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Dr. J V Tyagi
M.Sc. Ph D. (Chemistry) |
Dr. J V
Tyagi is M. Sc. Ph D. (Chemistry) by academic
qualification and having 26 years professional
experience. He has worked for 13 years in a Research
Centre of international repute and worked on various
research projects in the field of polymers, textiles
and environmental sciences. He has several
publications and papers to his credit in various
national and international seminars, workshops and
patents. He also worked at Shriram Applied Radiation
Centre as Assistant Director & Chief. Dr.Tyagi has 13
years of experience in various medical devices
manufacturing companies as Vice President
(Operations).
Dr. J V Tyagi is also approved Manufacturing Chemist
by FDA for the drugs under Schedule C & C1 and drugs
other than those under Schedule C & C1 under the Drugs
and Cosmetics Act. He is well versatile with the
requirements of various applicable national /
international statutory and regulatory requirements.
Dr.Tyagi has also vast experience for new products
design & development, process control, validation &
verification. He has been enormously involved in
monitoring suppliers’ performance, personnel training
and skill development, customer complaints, product
recall, advisory notices and QMS implementation. Dr
Tyagi has special expertise on various types of
sterilization processes including microbiological
aspects. He has also provided the requisite technical
inputs to the concerned functions relating to product
and process control and development. |
Dr. Tyagi has widespread
experience in documentation, implementation and
maintenance of GMPs and ISO QMS. He has also immense
experience in auditing ISO QMS certifications. He has been
member of Technical Committee of BIS (formerly ISI). Dr
Tyagi is a Qualified Auditor for ISO 9001 & ISO 13485 and
Medical Device Directive Expert on various international
certification & notified bodies like Det Norske Veritas,
Norway, British Standard Institution, UK, Standards
Australian Institution, Australia and Nemko, Norway. He
has audited more than 100 diversified medical devices
manufacturing companies for ISO 9001, ISO 13485 & Product
Certification i.e. CE Mark. He has more than 300 audit man
days to his credit He was also qualified Radiation Safety
Officer by BARC, Mumbai.
Presently, Dr. J V Tyagi is working as Technical Director
and CEO of Medical Division of Sahajanand Laser Technology
Limited. Sahajanand Laser Technology Limited is the
Manufacturer of laser marking & engraving, laser cutting,
laser welding, solar cell scribing/micro machining system
in industrial segments and portable CO2 laser unit with
different accessories (probes) by its brand name La-O-flex
CO2 Laser meant for various surgical applications. SLTL
enjoys its leadership into Jewellery Hallmarking segment
with over 60% market share. The company has planned for an
I.P.O for its renewable energy project. SLTL is coming up
very soon with a state-of-the-art manufacturing facility
for coronary vascular stents, drug eluting stents, PTCA
balloon catheters and stent delivery systems. The PTCA
balloon catheters will be now manufactured for the first
time by an Indian company indigenously i.e. Sahajanand
Laser Technology Limited.
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Mr. Himanshu Baid,
Managing Director,
Polymedicure Ltd. |
Mr
Himanshu Baid is the Managing Director of Poly
Medicure Ltd ( POLYMED ) .POLYMED was conceived and
established by a group of technocrataes making the
benefit of modern healthcare available to the mankind
at affordable price. This unique philosophy has been
the driving force behind he company since its
inception in 1995. Today it has grown into one of the
most dynamically versatile manufacturers of disposable
healthcare products in the region with over 40
different products.
POLYMED manufactures its products using state of the
art technology in ultra modern factories covering over
100000 square feet of manufacturing floor space with
about 10,000 square feet of clean rooms of class
100,000 to class 100. A tool room with modern
facilities & CNC machine supports the production
processes. A high degree of automation and an
effective process control help in complying with GMP
requirements. |
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