Volume 2 - Issue 1 provides insights into the articles belonging to the present time in International Journal of Pharmacovigilance. Being an Open Access Journal of Ophthalmology allows immediate and free access to PDF & HTML versions of published articles.
Volume 4 - Issue 2 provides insights into the articles belonging to the present time in Journal of Surgery. Being an Open Access Journal allows immediate and free access to PDF & HTML versions of published articles.
Similar to any other system, this system, too, is characterized by its processes, structures, and outcomes. For the sole purpose of good pharmacovigilance practices that provide guidelines on the pharmacovigilance system’s structures and processes, the quality of this system can be defined by the characterized system that produces relevant outcomes based on the pharmacovigilance objectives.
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Head of Pharmacovigilance Department, State Pharmacological Center, Ministry of ... Kava products. Regulatory decisions (due to drug safety information) ...
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Implementation is not the same in all MS. Complex system with many players. Duplication of work ... Consistency of law throughout the EU territory is ...
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Research Programme on Biomedical Informatics (GRIB) Ferran Sanz GRIB Ferran Sanz GRIB What is the GRIB? GRIB is a research programme of both Universitat ...
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Requirements for manufacture. Manufacturing authorisation issued by national ... Inspection of manufacture. The European Medicines Regulatory Networking Model ...
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Drug-related problems causing admission to a medical clinic. ... to a medical clinic. Eur J Clin ... An area for Clinical Pharmacology. 39. Take Home messages: ...
Estimates based on the number of vaccine doses distributed can be used for rough ... receive rotateq during the same period. No information on other differences between groups ...
How closely tied are the regulatory authorities to pharmaceutical companies? ... Do pharmaceutical companies spin safety information to their own ends? ...
Solutions to the meet global requirements for public data disclosure An Overview of Trial Transparency Requirements * * * * * * * * * * * * * * Support for Data ...
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1977 Food and Drug Administration (FDA) issued proposed ... Change of posology of the IMP. Change of comparator. Statistical analysis. Substantial Amendments ...
Regenerative medicine in Europe: political conflicts, economic biases, and legal loopholes Alex Faulkner Centre for Global Health Policy University of Sussex
New regulation for paediatric medicinal products issues and opportunities-Hans St tter MD Internal Medicine + Oncology/Haematology Clinical Reviewer Division ...
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The Italian Bio-Metacluster a key industry and research sector in three local areas ... virus-like-particles; the adjuvant effect of different cytokines; development ...
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Medical Informatics Perspectives on Leveraging the Electronic Medical Record in Pharma ... Has been nearly invisible to pharma for numerous reasons, largely due to ...
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Addressing the Barriers to Effective Pain Management and Issues of Opioid Misuse and Abuse Maureen F. Cooney, DNP, FNP Adjunct Faculty, Family Nurse Practitioner Program
Used by drug companies as marketing(!) FDA Phase IV requirement is the exception, not the rule ' ... Drug companies can NOT promote their meds for off label uses ...