CRO Quality Charcoal DFI Ocular tolerability Phase I Unit CDM IEC Gynaecological trials HTA ICF Phase I Steady state Hypothalamic AGAH Clinical trials Postmenopausal women Ophthalmologist Xerostomia Pharmacokinetics Children DUS GCP training Drug Food Interaction In vitro in vivo correlation US FDA EMA Hormone replacement therapy Post authorisation Phase II Life cycle management Rhine Main area Local tolerability Clinical study ANVISA Early phase Common cold Design development Eye disease Feasibility Auditing Expert Thuringia Good Clinical Practice Dry powder inhaler Cough DDI Data management Training Data Management Plan Female adolescents Endpoint Monitoring US CFR 21 Part 11 Healthy subjects Dermal irritation CDISC CRA Contraception IVIVC Pilot study Authorities Recruitment rates PAES Metered dose inhaler Allergy Transdermal therapeutic system Dry eye Legal Information Scientific advice Adrenocortical Cardiovascular surveillance First in human Axis Quality Assurance Experience Protocol PASS Scientific expertise Spacious archive Database DPI CDASH Subcontractor qualification Phase IIa trials Oncologic network Centralised procedure WinNonlin Pharmacodynamic studies Non interventional Inhalatives Creativity Project Management Bioequivalence Patch adhesion Legal representative Investigators brochure Biopharmaceutics Sample size estimation Edema Biopharmaceutical Ophthalmology HRT Clinical pharmacology unit SocraTec C&S IMPD Product development MMM Absorption Source Data Verification Pharmacology Pragmatism COPD Audit Bioavailability HPA axis NIS Sensitisation trials Pituitary Immunogenicity Clinical development program Data Validation Plan Pharmacokintetics Uveitis Ovulation inhibition CRF Safety FIM Sore throat Oncology Macular Oncological patients Slit lamp microscopy Patient recruitment Patients MCID Statistical programming Statistical services OTC Ophthalmological trials Glaucoma Asthma Anaesthesiologist IB Biosimilars Consultancy Protocol development Clinical Monitoring Inspection Lung SAS Competence Elpro Informed Consent Procedure Intensive assessment station Efficacy TTS GLP Paediatricians CDSIC Patch Phase IV Pulse oximetry plethysmography Drug Drug Interaction Biometrics Highly variable drugs Quality Management System ADAM Referral system Standard operating procedure Phase III Statistical Analysis Plan SDV Phase IIb trials SOP based Sequential designs MDI Standardisation FDA GCP Degeneration Copyright Network Absorption windows Dose linearity Central surveillance system
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Biostatistics
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Expert Statement
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Expertise
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Pharmacokinetics
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Oncological trials
Box 15
Ophthalmological trials
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Inhalatives
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Children
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Sexual Hormones
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Therapeutic Expertise
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Clinical Development
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Phase I
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Phase II / Proof of Concept
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Phase III in OTC
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Phase III
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Non-Interventional
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Magnetic Marker Monitoring
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Medical Devices
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Nutrition Studies
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Clinical Pharmacology Unit
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German Pharm-Tox Summit 2017 in Heidelberg
Box 50
2nd part of Introductory Course in Explorator...
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Introductory Course in Exploratory Medicines ...
Box 52
2nd Global Bioequivalence Harmonisation Initi...
Box 53
Quality Management Systems in Early Phase Tri...
Box 54
Trial in drug-induced xerostomia published
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The SocraTec Family
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SocraTec C&S
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