Milestones of success
Unless you try to do something beyond what
you have already mastered, you will never grow
OUR ACHIEVEMENTS
1981
Dr. Reddy
sets up the
Flagship
Company
Virchow
Laboratories
Ltd.
1992
Established
Saraca
Laboratories
with an aim to
manufacture
Bulk Drugs &
Intermediates.
1995
WHO GMP,
EU GMP
certification.
1998
Started
production of
Ranitidine HCL & in a short span
of time has
become one of
the largest
manufacturers
in the world.
2001
Launched the bio-pharmaceutical
company Virchow biotech focusing on
wide range of biological & biogenetics
by genetic engineering in consortium
with a group of biotechnologists
based at Vanderbilt University,
Nashville, TN, USA.
EDQM
certification.Became largest
producer of
Sulfamethoxazole
with an output of
400 MT per annum.
Services more than
90% of the worldwide
Sulfamethoxazole
requirement.
2002
Acquired Covalent
Laboratories (P) Ltd,
a multi-product
with GMP certified
Cephalosporin API
manufacturing facility
with a capacity of 240 MT of Cephalosporin API.
2003
US FDA Approval.
2005
First to
commercialise in
India the bio-generic
of the only genetically
engineered product for
wound healing PDGF
to have been approved
by USFDA.
2007
First to launch
indigenous
generic PTH
Teriparatide and
Interferon & Peg
interferon in India.
Launched dedicated
Advanced Wound
Care division to market
PDGF, Hemostats,
and unique SAP (Sub
atmospheric pressure)
therapy.
2008
Launched
Virchow
Healthcare Ltd,
focusing on the
growing global
emerging
market needs.
Signed MOU with then
no.2 Pharma Company in
India to market Virchow’s
indigenously developed
recombinant therapeutic
protein for osteoporosis
treatment and Interferon,
Pegylated Interferon & Ribavirin
for Hepatitis management.
2011
Out-licensing
agreement with
leading Pharma
companies to
market biotech
range.
2012
Launched domestic marketing
arm under the banner
of flagship company Virchow
Laboratories Ltd with cost effective,
quality solutions for complete
Hepatitis and Osteoporosis
management. |