• Clinical Trial Project Management
  Lotus Labs offers a proactive client-centric account clinical project management approach to provide complete program management for our clients with personalized focus on deliverable.
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• CRO’s help in Medical Innovation and Drug Development
  Serious medical conditions like the new threats that result from chronic ailments and their critical conditions need fast responses and continuous attempts in a huge scale and on a global level.
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• DCGI not to approve BA/BE studies conducted at clinical or bioanalytical facilities not approved by CDSCO
  The drug controller general of India (DCGI) will not accept and approve the reports of bioavailability (BA) and bioequivalence (BE) studies which are conducted at clinical or bioanalytical facilities that are not approved by the Central Drugs Standard Control Organisation (CDSCO).
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• Essential Aspects that Influence Contemporary Clinical Trials
  To explain in simple terms, clinical trials are important steps to arrive at a new treatment procedure for severe diseases.
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• Essential Components of Clinical Trials
  Clinical trials can be defined as a set of drug development and medical research procedures that generate data efficacy and safety.
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• European Commission issues GDP norms,Indian pharma conform to new rules
  European Commission has issued a guidance on Good Distribution Practice (GDP) of edicinal products for human use. Indian pharma companies see the new norms would transform the pharma marketing in the region.
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• Functions of Regulatory Compliance Services in CRO’s
  The Indian subcontinent in the last decade has witnessed multiple developments and advancements in clinical trials and in data and project management.
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• How Does Clinical Laboratory Services Help in Clinical Trials?
  A clinical research is incomplete without a clinical laboratory. Simply put, a clinical laboratory recognizes the chemical composition in blood samples and urine.
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• Implications of Clinical Laboratory Quality and Services
  Clinical laboratory quality control is a discipline to detect, minimize and correct the deficiencies present in the laboratory’s internal analytical process before the releasing the patient results, to enhance the quality of results that are reported by the laboratory.
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• Importance of Biometrics Research & Services in Clinical Trials
  Biometrics is also termed as biometry or biostatistics. Clinically, it is the application and development of mathematical and statistical processes to analyze the data that is an outcome of biological observations and phenomena.
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• Improve Medical Care and Treatment through Clinical Trials and Research
  Wikipedia defines clinical trials as "sets of tests in medical research and drug development that generate safety and efficacy data (or more specifically, information about adverse drug reactions and adverse effects of other treatments) for health interventions (e.g., drugs, diagnostics, devices, therapy protocols)."
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• Innovative Biometrics Solutions that CRO’s Provide
  The fast changing medical sphere has its own needs that are important but varied in nature. In addition to that there are also needs that should be catered for the smooth functioning and proper medical development.
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• Late Phase Clinic Research Trials
  The team for Late Phase Study at Lotus Labs comprises of experienced & target oriented group of Clinical Research professionals that are well trained to effectively manage timelines & ensure the required quality standards in Late Phase Study.
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• Late Phase Clinic Research Trials
  The team for Late Phase Study at Lotus Labs comprises of experienced & target oriented group of Clinical Research professionals that are well trained to effectively manage timelines & ensure the required quality standards in Late Phase Study.
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• Late Phase Clinical Trials
  Late phase studies :At Lotus Labs, the Late Phase studies portfolio offers comprehensive management and monitoring through:Project Management, feasibility / Site, Selection/ Study Management, Clinical Trial monitoring, Data Management and more. Lotus has well experienced team to handle Late phase studies. The sites involved in Late phase studies/Clinical trails have been audited by regulatory agencies including FDA.
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• Late Phase Clinical Trials
  Late phase studies :At Lotus Labs, the Late Phase studies portfolio offers comprehensive management and monitoring through:Project Management, feasibility / Site, Selection/ Study Management, Clinical Trial monitoring, Data Management and more. Lotus has well experienced team to handle Late phase studies. The sites involved in Late phase studies/Clinical trails have been audited by regulatory agencies including FDA.
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• Late Phase Clinical Trials
  Late phase studies :At Lotus Labs, the Late Phase studies portfolio offers comprehensive management and monitoring through:Project Management, feasibility / Site, Selection/ Study Management, Clinical Trial monitoring, Data Management and more. Lotus has well experienced team to handle Late phase studies. The sites involved in Late phase studies/Clinical trails have been audited by regulatory agencies including FDA.
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• Medical Writing Services Offered By CRO’s
  With the medical landscape progressing leaps and bounds, medical writing has evolved as a separate field and so have the medical writers.
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• Nearly 500 ethics committees registered after CDSCO made it mandatory in Feb, 2013
  Evoking a very good response to the steps by the regulatory authorities to streamline the clinical trials sector, nearly 500 ethics committees of hospitals and clinical trial organisations have secured registration within just five months after it was made mandatory
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• Need and Features of Regulatory And Compliance Services
  With rigid timelines and critical regulatory documentation methods, carrying out a clinical trial quickly is generally easy only in theory than reality.
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