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Forming Alliances to forge ahead
SIRO Clinpharm and Virginia Contract Research Organization
Pact enables SIRO’s clients access to booming Taiwan clinical research market
VCRO is one of the most experienced CROs with the longest history in Taiwan’s contract research sector. VCRO is dedicated to offering
full range ICH-GCP compliant clinical research services including EDC, IVRS and analytical laboratory services for pharmaceutical and biotech
companies. They have an extensive network in the Asia-Pacific regions of Japan, China, Singapore and Hong Kong.
This alliance is a collaborative partnership and will help us deliver value arising out of clinical capabilities and wider geographies to our global
set of clients.
SIRO Clinpharm and DreamCIS
Pact will broaden SIRO’s reach in Asian Clinical trials sector
DreamCIS is a South Korea based CRO with close to a decade’s experience in offering clinical
research services to pharmaceutical companies, bio venture companies, medical device manufacturers, and
functional food producers. Their services range includes Clinical trial management, Pharmacovigilance,
Post Marketing Surveillance (PMS), Data management, Biostatistics and Quality Assurance services.
This partnership is ideally created to provide a sustainable value for our existing as well as potential
customers in the rapidly growing Korean clinical trials market.
SIRO Clinpharm and Mediscis Medical Science Services
Alliance will expand SIRO's reach in Western Europe Early Phase Clinical Research Market.
Mediscis is a France based Clinical Research Organization. Mediscis is an established expert in GCP compliant
early phase drug development services including clinical trials and bioanalytics; SIRO offers expertise across all
study phases for the pharmaceutical and biotech industry. Mediscis is based in Poitiers and La Rochelle,
France.
This alliance will allow SIRO to provide additional services to global clients to support their clinical
development plans.
SIRO Clinpharm and CambReg Ltd
Alliance will offer a one stop solution to pharmaceutical companies looking to
register their products in the lucrative European markets.
CambReg, established in 1999 is a full service regulatory services company based in Cambridgeshire,
UK. It helps pharmaceutical and biopharmaceutical companies with regulatory affairs advice, submissions and
compliance. It has provided services to over 200 clients based in Europe, America and Asian countries. The
founder directors are exhealth authority staff and have over three decades of experience with European
regulatory affairs.
The alliance will offer full scope regulatory services to companies wishing to register human medicines of any
kind including new small molecule or biotech entities, Biologics and Herbals as well as Generics. Services
include preparing CTAs, MAAs in eCTD format, PIPs, PUMAs, etc and managing DCP/MRP across whole of the EU as
well as consultancy for any issues with regulatory authorities.
SIRO Clinpharm and Advanced Clinical Trial Solutions
Alliance provides global Oncology Clinical development solutions in North America,
Europe and India.
Advanced Clinical Trial Solutions LLC (ACT Solutions.) is a privately held company that is devoted to
operational excellence in global oncology drug development. ACT Solutions is staffed solely with experienced
oncology personnel that has enabled it to grow its business annually and to establish strategic partnerships to
expand the scope of the ACT Solutions service offerings.
This alliance has enabled SIRO to expand its Oncology Clinical development and patient recruitment expertise to
North America. ACT Solutions and its clients benefit by gaining access to SIRO’s clinical study management,
patient recruitment, data management, biostatistics and medical writing capabilities in India and European
countries.
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