The Target Health Global Partnership (THGP) brings together the "best of the best"
small to mid-size companies from all corners of the world to offer the most sophisticated
and experienced approaches to drug, biologic and device development. Our partners
include:
- EHR/EDC Integration
- CLINICAL RESEARCH
- Regulatory Consulting
- Analytical Methods
- Statistics
EHR-EDC Integration - For more information contact
Warren Pearlson
- Life on Key http://www.lifeonkey.com
LifeOnKey™ is a leader in the health information technology industry. Through
its web-based solution, LifeOnKey™ transforms the way health information is
collected, managed and analyzed, enabling major stakeholders in the health care
system – physicians, hospitals, patients, clinicians – to aggregate and exchange
medical data securely and efficiently. LifeOnKey's three primary applications –
an EHR, a PHR and the Research Center – are seamlessly integrated, delivering relevant
data that can be refined and targeted to the needs of each unique user. The company
currently has 1.5 million patient users globally. LifeOnKey's headquarters are located
in New York and its R&D in Herzliya, Israel.
CLINICAL RESEARCH - For more information contact
Warren Pearlson
- The Clinical Research Center http://www.tasmc.org.il/e/398/ - Israel Phase I/IIA
The Clinical Research Center is an Early-Phase Clinical Pharmacology Unit located
at the Tel-Aviv Sourasky Medical Center (TASMC The CRC combines the capability of
carrying out Phase-I and bioequivalence studies involving healthy volunteers as
well as Phase IIA studies with patients from the various hospital disciplines. The
personnel operating the CRC are trained to GCP standards.
Since its establishment, the CRC has successfully undertaken clinical studies for
both Israeli and international pharmaceutical companies in a broad range of therapeutic
areas.
- CTG (Clinical Trials Group) http://www.ctgcro.com - European Clinical Trials
CTG (Clinical Trials Group) is a private contract research organization (CRO) experienced
and specialized in conducting all phases (I-IV) clinical trials. CTG's team has
developed expertise in managing clinical research in a broad range of therapeutic
areas:. CTG's primary goal is to deliver high quality data to its customers. With
an experienced and reliable team on board, CTG is a trusted partner in clinical
research which is enforced by high working standards of Quality Control (QC) and
Quality Assurance (QA).
- IATEC
http://www.iatec.com/ - Global Clinical Trials
IATEC has been involved in over 150 projects in the last 5 years, of which 23 were
full service projects with over 2300 subjects in 20 countries and 320 sites. Other
projects include submission and monitoring services, consulting and statistical
and data management services.
- KCR http://www.kcrcro.com/
- European Clinical Trials
KCR is a leading European CRO with headquarters in Warsaw, Poland. KCR has 10 offices
across Central and Eastern Europe and our own staff in all CEE countries.
Since 1997 KCR has carried out more than 300 clinical trials treating nearly 300
000 patients at more than 7500 sites. We have extensive experience in conducting
clinical trials for pharmaceutical, biotechnology, medical device and food supplement
companies. KCR offers clinical research services from phase II to phase IV within
a broad range of therapeutic areas. KCR is the preferred CRO Partner for some US
and EU pharmaceuticals and biotechnology companies.
- LSK Global Pharma Services Korea http://www.lskglobal.com/ - Asian Clinical trials
LSK Global PS is one of major local Korean CROs providing the entire range of services.
Numerous pre-study assessments by global sponsors and CROs have qualified LSK as
a global level. It has a strong relationship with the Korean FDA and major investigational
sites. LSK is collaborating with a number of global CROs.
Regulatory Affairs - For more information contact
Warren Pearlson
- Granzer Regulatory Consulting Service http://www.granzer.biz/ - European Regulatory Consulting
Granzer Regulatory Consulting & Services, we facilitate the life of our customers
by helping to provide strategic and operational input into drug and device development
and all elements of regulatory affairs including a sound regulatory strategy.
- LSK
http://www.lskglobal.com/ - Asian Regulatory Consulting
Regulatory strategy consulting, filing assistance LRD (Local Registration Dossier,
Korea) and IRD (Int'l Registration Dossier, East Asia.
- Voisin Consulting http://www.voisinconsulting.com/ - European Regulatory Consulting
Voisin Consulting assists biotechnology, pharmaceutical and medical technology companies
in the design and implementation of innovative and global regulatory strategies
in order to expedite product development.
Analytical Methods - For more information contact
Warren Pearlson
- Microconstants http://www.microconstants.com/ - Bioanalytical & Pharmacokinetic
Analysis
MicroConstants is a GLP-compliant Contract Research Organization (CRO) dedicated
to providing premier quality bioanalytical, pharmacokinetics, drug metabolism, formulation
analysis and immunoassay support services to pharmaceutical and biotech companies
worldwide.
Statistics - For more information contact
Warren Pearlson
- BrightTech International http://brightech-intl.com/ - Biostatistics China
BrightTech provides high services in statistics, SAS programming, medical writing,
data management and clinical operation for pharmaceutical and market research companies.