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Showing below up to 50 results in range #1,001 to #1,050.

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  1. Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - inspection (6 links)
  2. Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - patient/subject file (6 links)
  3. Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - protocol (6 links)
  4. Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - serious adverse event (6 links)
  5. Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - witness (6 links)
  6. Reference:WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 Page 22 (6 links)
  7. Reference:WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 Page 31 (6 links)
  8. Reference:WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 Page 44 (6 links)
  9. Reference:WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 Page 78 (6 links)
  10. Reference:WMA Declaration of Helsinki 2024 - (6 links)
  11. Reference:WMA Declaration of Helsinki 2024 34 (6 links)
  12. Reference:WMA Declaration of Helsinki 2024 Paragraph 17 (6 links)
  13. Reference:WMA Declaration of Helsinki 2024 Paragraph 22 (6 links)
  14. Reference:WMA Declaration of Helsinki 2024 Paragraph 23 (6 links)
  15. Reference:WMA Declaration of Helsinki 2024 Paragraph 23 - Final report (6 links)
  16. Reference:WMA Declaration of Helsinki 2024 Paragraph 23 - Oversight (6 links)
  17. Reference:WMA Declaration of Helsinki 2024 Paragraph 29 – 30 (6 links)
  18. Glossary:TAG-00058-Eur-zne (6 links)
  19. Glossary:TAG-00067-Exp-war (6 links)
  20. Glossary:TAG-00076-Fea-ung (6 links)
  21. Glossary:TAG-00082-Scr-hlu (6 links)
  22. Glossary:TAG-00138-Rem-oni (6 links)
  23. Glossary:TAG-00140-Ris-nRi (6 links)
  24. Glossary:TAG-00218-Har-päi (6 links)
  25. Glossary:TAG-00232-Per-die (6 links)
  26. Glossary:TAG-00248-Inv-die (6 links)
  27. Glossary:TAG-00259-AEs-ten (6 links)
  28. Glossary:TAG-00264-Eud-lin (6 links)
  29. Glossary:TAG-00267-Wit-mmi (6 links)
  30. Glossary:TAG-00273-Fin-den (6 links)
  31. Glossary:TAG-00279-Hea-rFr (6 links)
  32. Glossary:TAG-00288-Qua-nag (6 links)
  33. Glossary:TAG-00302-Ada-die (6 links)
  34. Glossary:TAG-00303-Int-lan (6 links)
  35. Glossary:TAG-00309-Rea-eal (6 links)
  36. Glossary:TAG-00312-Imp-isi (6 links)
  37. Glossary:TAG-00323-Pau-Imp (6 links)
  38. Glossary:TAG-00331-Une-irk (6 links)
  39. Glossary:TAG-00345-Cou-ngs (6 links)
  40. Document:DEU Empfehlungen des BfArM und des PEI zur Europäischen Guidance during COVID-19 v4 04-Feb-2021 (5 links)
  41. Document:DEU Richtlinie zur Bewertung der Qualifikation von Prüfern, Hauptprüfern, Leitern und ärztlichen Mitgliedern von Prüfungsteams durch Ethik-Kommissionen von Arbeitskreis Medizinischer Ethik-Kommissionen in der Bundesrepublik Deutschland e. V. und (5 links)
  42. Document:EU COMMISSION IMPLEMENTING DECISION (EU) 2022/729 11-May-2022 (5 links)
  43. Document:EU EMA/431265/2016 Annex I – to guidance for the conduct of good clinical practice inspections – investigator site 06-Sep-2017 (5 links)
  44. Document:EU EMA/INS/GCP/143492/2022 - ANNEX I TO PROCEDURE FOR CONDUCTING GCP INSPECTIONS REQUESTED BY THE CHMP: INVESTIGATOR SITE 2022 (5 links)
  45. Document:EU Regulation (EC) No 726/2004 - authorisation and supervision of medicinal products for human use 28-Jan-22 (5 links)
  46. Document:FRA AEC DOC010 V.04 01-Jun-2018 (5 links)
  47. Document:FRA Bonnes pratiques - CONTRÔLE QUALITÉ À DISTANCE DES ESSAIS CLINIQUES (CNIL) 16-May-2024 (5 links)
  48. Document:FRA SURV VIG DOC118 V01 REC-Avis aux promoteurs -Partie V 16-May-2025 (5 links)
  49. Document:GBR Clinical investigations of medical devices – compiling a submission to MHRA May 2021 (5 links)
  50. Document:GBR Guidance Managing clinical trials during Coronavirus (COVID-19) 16-Nov-.2021 (5 links)

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