1. (2022) Results.Healthcare, CRO sector, M&A drivers and market trends. https://resultsig.com/wp-content/uploads/2022/02/CRO-sector-MA-drivers-and-market-trends-Q1-2022-Results-Healthcare.pdf. Zugegriffen: 9. Aug. 2022
2. EU Commission Clinical Trials Regulation CTR. https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=celex%3A32014R0536 (Erstellt: 16. Apr. 2014). Zugegriffen: 9. Aug. 2022
3. EMA CTIS Sponsor Handbook, v2. https://www.ema.europa.eu/en/human-regulatory/research-development/clinical-trials/clinical-trials-information-system-training-support#handbook-for-clinical-trial-sponsors-section (Erstellt: 30. Nov. 2021). Zugegriffen: 9. Aug. 2022
4. EMA EMA CTIS Online Training Program, Management of registered users and role matrix (Module 7), v1.45 – März 2022, Sponsor Business Processes and roles. https://www.ema.europa.eu/en/documents/other/sponsors-business-processes-roles-ctis-training-programme-module-07_en.pdf. Zugegriffen: 9. Aug. 2022
5. EMA Draft Guidance on how to approach the protection of personal data and commercially confidential information in documents uploaded and published in the Clinical Trial Information System (CTIS). https://www.ema.europa.eu/en/documents/other/draft-guidance-document-how-approach-protection-personal-data-commercially-confidential-information_en.pdf (Erstellt: 7. Apr. 2022). Zugegriffen: 9. Aug. 2022