One of the 'Unique' move made by the Ministry of Health of Catalonia is establishing 'Record' keeping system for all the Healthy Volunteers participating in Phase 0 or Phase I Clinical Trials,thus ensuring Safety and well being of Human Subjects taking part in Clinical Trials.Ministry of Health had released a Document called ' Medical and Technical Requirements for Units Conducting Clinical Trials with Medicinal Products used for Non Therapeutic Purposes for the Participants'.in the year 2003.There was an emphasis on Training of the staff Involved in Clinical Research activities,good Infrastructure at the facility conducting a Trial etc.
Helix will be exploring the possibilities of working in the Spanish Bioregion Network,consisting of Bioregions such as Biobasque,Catalonia,Bioval,Madrid,Andalusia and upcoming Bioregions in Canarias,Extremadura,Aragon,Navarra and Balearic Islands;making Barcelona as its main office for Catalan Speaking region.
The Medical Research and GCP Training Services being launched by Helix include; GLP and Non GLP Pre Clinical Research Services,Bio Availability & Bio Equivalence Studies,Phase 0 through IV Trials,Research Audits,Medical Writing,Regulatory Affairs,Quality Assurance,Clinical Data Management,Imaging,Clinical Trial Monitoring,Biostatistics,Pharmacovigilance,Translation,Site Management/Site Support/Trial Management,Imaging,GCP Training for Research Nurses,Principal Investigators/
The Founder Helix being a Doctor ,is always keen to promote Preventive Healthcare and Reinforce the efforts of Healthcare providers to fulfill WHOs Slogan ' Health For All'.Helix Research Center ,firmly believes in utilisation of Local Resources and continually Nurtures the talent of aspiring Life Sciences Graduates,Post Graduates,PhDs etc to become 'Indispensable' Clinical Research Professionals.This is an era of Public Private Patnerships,Cooperation and Collaboration and Helix is keen to make this a reality.
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Helix Research Center Ltd is a London(UK) based global company offering Contract Research,Training,Auditing,Consulting,Medical Writing,Pharmacovigilance,Biostatistics,SMO,Regulatory Affairs,Quality Assurance,Publications,Translation ,CDM services globally