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