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ICH Adopts Update to GCP Guideline; Regional Guidances to Follow

  • Post author:Sam
  • Post published:December 13, 2016
  • Post category:International Pharmaceutical Regulatory Monitor

The International Council for Harmonisation adopted an update to its good clinical practice guideline, recommending approaches to clinical trial design and management, as well as ensuring patient protection and data…

Continue ReadingICH Adopts Update to GCP Guideline; Regional Guidances to Follow

FDA Cites Japanese Drugmaker for Data Falsification

  • Post author:Sam
  • Post published:December 13, 2016
  • Post category:International Pharmaceutical Regulatory Monitor

Japanese drugmaker Sekisui Medical Co., Ltd has received a warning letter after an inspection in June revealed significant data integrity issues. Source: International Pharmaceutical Regulatory Monitor

Continue ReadingFDA Cites Japanese Drugmaker for Data Falsification

EMA Takes Steps to Implement ISO Standards for Drug Identifiers

  • Post author:Sam
  • Post published:December 13, 2016
  • Post category:International Pharmaceutical Regulatory Monitor

The EMA has released guidance on the first steps it will take to prepare drug sponsors to comply with new data standards for the unique identification of drugs set to…

Continue ReadingEMA Takes Steps to Implement ISO Standards for Drug Identifiers

China’s FDA Verifies Data from 55 Clinical Trials in First Audits

  • Post author:Sam
  • Post published:December 13, 2016
  • Post category:International Pharmaceutical Regulatory Monitor

As part of its clinical trial data auditing initiative, the Chinese Food and Drug Administration verified data from an initial set of 55 clinical trials, focusing mainly on large, international…

Continue ReadingChina’s FDA Verifies Data from 55 Clinical Trials in First Audits

FDA Strengthens Guidance on Quality Agreements with CMOs

  • Post author:Sam
  • Post published:December 13, 2016
  • Post category:International Pharmaceutical Regulatory Monitor

Three years after issuing proposed guidance that laid out the FDA’s expectations for quality agreements with contract manufacturers, the agency has firmed up and expanded what sponsors must do to…

Continue ReadingFDA Strengthens Guidance on Quality Agreements with CMOs

Indian Authorities Report 27 Drugs Failed Quality Tests

  • Post author:Sam
  • Post published:December 13, 2016
  • Post category:International Pharmaceutical Regulatory Monitor

Indian drug regulators in seven states have accused 18 drugmakers of selling substandard therapies after quality tests identified a range of product issues ranging from deceptive labeling to inappropriate quantities…

Continue ReadingIndian Authorities Report 27 Drugs Failed Quality Tests

EMA: Less Data Required for Expanding Orphan Drug Indications

  • Post author:Sam
  • Post published:December 13, 2016
  • Post category:International Pharmaceutical Regulatory Monitor

The European Medicines Agency published new guidance on whether less comprehensive data can be used to support a new indication for a previously approved orphan drug product. Source: International Pharmaceutical…

Continue ReadingEMA: Less Data Required for Expanding Orphan Drug Indications

Drugmakers Criticize German Proposal to Set Drug Price Ceiling

  • Post author:Sam
  • Post published:December 13, 2016
  • Post category:International Pharmaceutical Regulatory Monitor

Drugmakers have expressed concern about the German government’s proposal to restrict drug pricing — contending that the measure penalizes research and development. Source: International Pharmaceutical Regulatory Monitor

Continue ReadingDrugmakers Criticize German Proposal to Set Drug Price Ceiling

EMA: Comparative Studies Not Required for Heparin Biosimilar

  • Post author:Sam
  • Post published:December 13, 2016
  • Post category:International Pharmaceutical Regulatory Monitor

The development process for biosimilar heparins no longer requires a comparative clinical trial, according to new guidance from the European Medicines Agency. Source: International Pharmaceutical Regulatory Monitor

Continue ReadingEMA: Comparative Studies Not Required for Heparin Biosimilar

EMA Finalizes Guideline on Active Chemical Substances

  • Post author:Sam
  • Post published:December 13, 2016
  • Post category:International Pharmaceutical Regulatory Monitor

The European Medicines Agency adopted a final guideline setting out the information required for the evaluation of active chemical substances used in drug products. Source: International Pharmaceutical Regulatory Monitor

Continue ReadingEMA Finalizes Guideline on Active Chemical Substances
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