Global Reach
LIG-IAGIM
Drug Development Association signed close to a 190 generic drug
development projects in the 4Q of 2009 and 1Q -3Q of 2010 with
generic and innovative drug houses as diverse and far apart
as Argentina, Brazil, Canada, China, Denmark, Egypt, France,
Germany, Jordan Iran, Ireland, Malta, Malaysia, Mexico, Saudi
Arabia, Singapore, South Africa, UK, US and New Zealand.
LocumGroup now fully operational paperless back-office contributed
significantly to the rapid and smooth high speed technology
transfer process and proved itself to be a winner in cost effective
IT process management. As a global print and electronic Journal,
Handbook and technology publisher Locum's Paperless e-Office
Systems developed and validated over the past five years include
rapid and effective auto-invoicing, and client auto-banking
to auto-shipping, goods tracking and notification. Included
in the paperless e-Office are automatic tax e-filing and staff
remuneration, e-insurance, e-pension, e-autobanking, e-salary
and e-filing features fully integrated from Locum's Cape Town
to Miami operations.
Technology
Leading
Generic and Innovative Drug Manufacturers purchased formulation
and development, scale-up, validation and commercial IT data,
including CMC and Analytical methodology and Bioavailability
data profiles from LIG- IAGIM Drug Development Association on
an expanding worldwide basis. An interesting development was
China's new emergence in purchasing original drug development
know-how
by non-state limited liability pharma companies such as Hainan
Poly Pharm.
Drug Development
Indian
pharma companies have extended and advanced their large drug
development product pipeline by purchasing LIG-IAGIM technology
dosage form specific handbooks and technical know-how. USV (India).
Incepta Bangladesh FamyCare (India) and Randbaxy (India) Wockhardt,
Jubilant Organosys (India), Microlabs (India), Tablets India
and Ind-Swift have acquired LIG-IAGIM Research and Development
technological handbooks and analytical methodology databases
covering pre-formulation to scale-up, and commercial manufacturing
utilizing IAGIM extended drug development benefit plus plans
ranging from periods of 5 -8- 10 years for generic and innovative
drug development.
Europe and ME
Product
development data in the Middle East region covered critical
aspects from formulation technology to large scale development
plans. Egypt (Amriya), Jordan (Advance Pharmaceuticals), Iran
and Saudi Arabia Jazeera Pharmaceutical Industries manufacturing
complex have expanded their modern manufacturing and development
facilities. Locum International technology including validated
full scale commercial batches in all the proposed marketing
strengths enabling companies to slash their generic pipeline
queue from 10 -15 months of time saved when compared to formulating
from scratch. Locum's advanced modern IT transfer technology
reached as far as Lambo (Belgium), Bedi and Fournier France,
Alpharma (Denmark), CryoPharma SA (Mexico), KRKA Slovenia, Indonesia's
Sanbe Farma (Bandung), Dr Esteces (Spain) Standard Chem and
Pharm (Taiwan) and on to eastern Europe via Ukraine's Hexal
operations in Kiev.
Workshops and Drug Development Expositions
[US EXPO]
IAGIM
continued to advance and spread it's state-of-the-art drug development
know-how and validated commercial sized manufacturing technology
to the four corners of the earth in approximately 110 countries.
A new development was highlighted in the P.R. of China (PolyPharm)
incorporating additional western high tech based technology
and guidelines. IAGIM conducted regular drug development formulation
seminars symposia and workshops in all five continents. The
annual CT and US drug development Exposition (CT, US EXPO) drew
in large interested clientele from every continent, as well
as major generic and innovative drug development companies,
research laboratories and big pharma consultants.
Asia Technology
India
has maintained its' status and lead as a major technology purchaser
of LIG-IAGIM information technology (IT) and drug development
know-how covering all aspects from A-Z of Locum's databases.
Major Indian drug houses such as Adjunta, Centaur Pharmaceutical,
CadilaPharm, GlaxoSmithKline (Philippines), Indoco, IPCA, JB
Chemicals and Pharmaceuticals, RatioPharm, Orchid, Cipla, Novartis,
Nicholas Piramal, Randbaxy, Strides Arcolabs, Sun Pharma, USV,
Wockhardt and Dr. Reddys have expanded their state-of-the-art
international level operations and advanced research, development
and manufacturing capabilities utilizing key aspects of Locum
International Group's generic and innovative drug development,
HPLC + UV validated analytical methodology, development e-SOP
and FDA and EU level commercial manufacturing technology to
their product export advantage..
Global Technology
Locum
International Research Ltd., is headquarters in Israel, Locum
International Inc. in Florida USA and Locum International Group
Switzerland. The Group is among the top pharmaceutical generic
pharmaceutical drug development company in the world. The company
researches and develops generic formulations, manufacturing
processes, scale-up and validation commercial sized procedures
and markets generic and innovative controlled release and sterile
pharmaceuticals as well as active pharmaceutical ingredients
know-how and technology, such as the neurobiological innovative
drugs (F-CRAB's, CMZ CR) worldwide in over a 175+ countries.
LIG provides and presents leading FDA and EU approved SOPs,
PAIs, analytical methods, ANDAs, dossiers, seminars, workshops
and conferences worldwide, covering both pharmaceutical and
neurobiology (F-CRAB's).
Neurobiological Development - F-CRAB's
/ CMZ CR
LI neurobiology development and experimental unit is currently
developing advanced default protein folding mechanisms and routes
for the F-CRAB RRMS drugs (relapsing remitting multiple sclerosis
family of drugs), which include the development of the second
generation Glatiramer Acetate Copoxane2
(COP2), with special reference
to the molecular weight spectrum (Av.25+nK daltons spread and
limits/10+nK->25+nK) of the truncated four amino-acid glatiramer
acetate complex, which has a significant batch-2-batch (B2B-SV+RSD)
synthesis variation, requiring advanced cGMP and QA/QC controls,
that differ significantly from the normal drug synthesis pathways,
especially in intermediate QA testing of the protected intermediates.
Impeccable cleaning validation, stringent controls of starting,
intermediate raw materials and solvents, resulting in significantly
tighter batch to batch variations and B2B RSD's and impurity
profiles, using special HPLC column and gel-filtration analytical
methodology techniques.
Innovative Research
Workshops, lectures and seminars on the F-CRAB RRMS drugs, their
development, synthesis, formulation, proposed default 'protein'
folding, HPLC / gel filtration analysis/A.M validation and associated
e-CTD/CTD specification / parameters are available as per advertised
timetable in both EU and the US journal series (Contact LIG).
The International Journal of Drug Development (IJDD Vol. 10/11)
and the International Journal of Drug R&D (IJDR&D Vol.
11/12) are the main current print venues in the International
Journal Series for publishing the ongoing F-CRAB RRMS drug innovation,
experimental research and product development. Other venues
include International Journal of Drug cGMP (IJGMP) and International
Journal of Drug Validation (IJDV) and International Journal
of Drug Master Formula and Processes (IJDM&P).
Market Highlights
Over
85% of Locum's technology sales are in Asia/China/Japan (39),
North America (31) and Europe (30).
For additional information contact LIGroup (www.LocumUSA.com)
or IAGIM (www.iagim.org) or use the LIG international
tel/voice messaging system US +1-561-865-6147
Pharma
Today, International Journal of Generic Drugs, Times of India,
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