• 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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• Need for Positive Clinical Research Programs For Better Medical Treatments
  Clinical research plays a vital role in the treatment discovery and drug development process. The new era hectic lifestyle has increased the frequency of chronic ailments globally.
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• Need for Regulatory & Compliance Services in Drug Development
  Medical regulatory & compliance services today is a dynamic business sector with an aim to get the products to the market within reduced cost, time and at a commercially feasible label.
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• Need of a Biotech Clinical Laboratory in Clinical Trials
  Keeping in mind the present day ailments and chronic diseases, the medical industry have gained immense significance. It is essential to keep the general mass free from disease and to arrive at advanced methods of drug development treatment and healing modalities.
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• New Age Uses of Healthcare Biometrics
  According to a report Transparency Market Research concentrating on the medical biometrics market estimates that the segment was valued at USD 1.2 billion in 2012 and is calculated to grow at rate of CAGR of 25.9% from 2013 to 2019, to go up to an expected amount of USD 5.8 billion in 2019.
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• Online Clinical Trials – Scopes for Mobile Enabled Clincial Trials Today
  The rapid development of internet and advancements in software technology is proving to be beneficial to the medical landscape in many ways.
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• Phase I Clinical Trial
  Phase I clinical trial : Lotus Labs leadership & a proven track record in the effective conduct of Phase I Clinical Trial is reflected in the fact that we have a strategic working relationships with reputed hospitals that ensures having access to a large database spanning diverse therapeutic areas.Lotus Labs has extensive capabilities to conduct Phase I Studies in healthy volunteers which include studies First-in-Man, Single ascending dose, multiple ascending dose and new chemical entities.
  in Public bookmarks with 1 clinical i phase phase-i-clinical-trial trial trials by 3 users
• Phase I Clinical Trial
  Phase I clinical trial : Lotus Labs leadership & a proven track record in the effective conduct of Phase I Clinical Trial is reflected in the fact that we have a strategic working relationships with reputed hospitals that ensures having access to a large database spanning diverse therapeutic areas.Lotus Labs has extensive capabilities to conduct Phase I Studies in healthy volunteers which include studies First-in-Man, Single ascending dose, multiple ascending dose and new chemical entities
  in Public bookmarks with 1 clinical clinical-trials-phase--1 i phase trial trials by 2 users
• Phase I Clinical Trial
  Phase I clinical trial : Lotus Labs leadership & a proven track record in the effective conduct of Phase I Clinical Trial is reflected in the fact that we have a strategic working relationships with reputed hospitals that ensures having access to a large database spanning diverse therapeutic areas.Lotus Labs has extensive capabilities to conduct Phase I Studies in healthy volunteers which include studies First-in-Man, Single ascending dose, multiple ascending dose and new chemical entities.
  in Public bookmarks with 1 clinical i phase trial trials by 3 users
• Putting Biometrics Technology to Advanced Usages
  Biometrics can be defined as a body of medical science discipline that has certain technologies and methods of approval of an individual using processes for automatically verification of personal traits, such as face, hands, fingers, voice and eyes using prints, geometry as well as pattern recognition.
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• Recent Developments in Biometric Identification Systems
  To elucidate in simple terms, Biometric identification systems are personal biological or physical scanning’s/measurements done about an individual.
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• Services Offered By Indian CRO’s
  India has been successfully able to provide cost savings of 50 to 60 percent in clinical trials. With the research discovery acquiring approximately one-third of the R&D expenses of the western medical industry, outsourcing to lesser expense countries is a wise move.
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• Significance of Regulatory Services in Clinical Trials
  According to GCP (Good Clinical Practice) research guidelines there is a certain standard for the conduct, design, monitoring, performance, recording, auditing, reporting and analyzing of clinical trials.
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• State-of-the-Art Phase I Clinical Trial Facilities
  Lotus Labs has independent Phase I clinical trial facility & the expertise to conduct First-In-Human Studies, Pharmacokinetic studies, Bio-availability & Bio-equivalence studies, Drug Metabolism studies, Dose Proportionality & Multiple dose studies & more.
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• State-of-the-Art Phase I Clinical Trial Facilities
  Lotus Labs has independent Phase I clinical trial facility & the expertise to conduct First-In-Human Studies, Pharmacokinetic studies, Bio-availability & Bio-equivalence studies, Drug Metabolism studies, Dose Proportionality & Multiple dose studies & more.
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• Understanding the Fundementals of Clinical Trials & its Phases
  Clinical trials are medical researches that are carried on utilizing human participants by researchers in medical schools, government labs, or by pharmaceutical manufacturers in order to review how a certain medical device, a new drug, therapy, diagnostic tool, treatment or a type of prevention is working to enhance patient health, cure ailment and enhance the overall quality of life.
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• US FDA issues norms on delaying a drug inspection,waits industry comments
  "The US FDA has issued guidance to the pharma industry on circumstances that constitute delaying, denying, limiting, or refusing a drug inspection. The regulatory major is seeking industry comments to this effect by September 30, 2013. "
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• US FDA issues rules on Electronic Source Data in Clinical Investigations;Indian CROs view it platform to prove proofs
  US Food and Drug Administration (FDA) has issued the guidance for industry on Electronic Source Data in Clinical Investigations. This guidance provides recommendations to sponsors, Contract Research Organisations (CROs), clinical investigators, and others involved in the capture, review, and retention of electronic source data in FDA-regulated clinical investigations.
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• US FDA norms for clinical investigators, sponsors & to ascertain need for human studies for IND
  "In a major development on the regulatory landscape for clinical trials, the US Food and Drug Administration (FDA) has now issued a guidance which is intended to assist clinical investigators, sponsors, sponsor-investigators and institutional review boards (IRBs)."
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• US FDA seeks industrys comments on new draft norms on ANDA submissions
  The US FDA has sought the pharma industry's comments on its draft guidelines on ANDA (abbreviated new drug application) submissions ― Refuse-to-Receive Standards.
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