ISSN: 0975-0851
Journal of Bioequivalence & Bioavailability
Open Access
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Relevant Topics
- Advances in Bioavailability
- Advances in pharmaceutical analytical methods
- Air analysis
- Anthropology Biomedicine
- Antigen â Antibody Reaction
- Anvisa Bioequivalence
- Anvisa regulatory guidelines
- Applied Biomedicine
- BA/BE Studies
- Bioanalysis Methods
- Bioanalytical Chemistry
- Bioanalytical Method Validation
- Bioequivalence Anticancers
- Bioequivalence Antidiabetics
- Bioequivalence Antidiuretics
- Bioequivalence Antipsychotics
- Bioequivalence Cardiovascular Products
- Bioequivalence Study Design
- Bioequivalence Study Protocols
- Biomedicine and Pharmacotherapy
- Biopharmaceutics
- Biosimilars
- British regulatory guidelines
- Cell genetics
- Chemical analysis
- Chromatographic Techniques
- Clinical Cancer Trials
- Clinical Drug Trial
- Competitive analysis of drugs
- Computational Biomedicine
- Drug Delivery using Nanotechnology
- Drug Designing
- Drug analysis
- Drug devices
- European Bioequivalence
- Europian regulatory guidelines
- Experimental Drug Trial
- FDA Bioequivalence
- Fragment Based Drug Design
- Heat Shock Proteins
- In Silico Methods
- In vitro Bioequivalence
- Japan regulatory guidelines
- Marine Biomedicine
- Mass Spectroscopy
- Medical Biology
- Medical devices regulations
- Molecular Biomedicine
- Molecular Epidemiology
- Molecular Modeling
- NMR Applications in Biomedicine
- Nano Medicine
- Nanomedicals
- Negative Results in Biomedicine
- Paid Clinical Trials
- Peptidomimetic
- Pharmaceutical analysis
- Pharmaceutical analytical market
- Pharmaceutical care
- Pharmaceutical companies and regulatory guidelines
- Pharmaceutical ethics
- Pharmaceutical formulation
- Pharmaceutical technology
- Pharmaceutics
- Product analysis and marketing
- Protease Substrate/Inhibitor
- Quality assurance in pharmaceutical analysis
- Quality assurance in regulatory affairs
- Receptor Agonist/ Antagonist
- Regulatory Requirements in Bioequivalence
- Regulatory affairs
- Regulatory affairs for clinical trails
- Regulatory compliance
- Regulatory consulting and market analysis
- Regulatory requirements of pharmaceutical products
- Regulatory services and market analysis
- Spectrometry
- Sports Biomedicine
- Structure Based Drug Design
- Systems Biomedicine
- US FDA guidelines
- Validation
- screening and Drug Design
Kun Fang Ma
Biography
Dr.Kun Fang Ma GR is currently working in School of Pharmacy at Nanjing Medical University, China.
Research Interest
Pharmacokinetics, Bioequivalence & Bioavailability.
Publications
Mei Juan Ding, Li Hua Yuan, Yun Li, Shu Wang, Xiao Li Wu, Jie Liu, Kun Fang Ma, Hong Wei Fan, Zhen Yu Lu, Hui Juan Xu and Xue Min Zhou
Research Article: JBB/Vol.3.2 032-037 (2011)
Global Speakers in the subject
Global Experts in the subject
Relevant Conferences
- Analytical Science and Separation Techniques
Euro Mass Spectrometry 2018 (Italy) - Applications of Mass Spectrometry
Euro Mass Spectrometry 2018 (Italy) - Chromatography and High Performance Liquid Chromatography (HPLC)
Euro Mass Spectrometry 2018 (Italy) - Fundamentals of Mass Spectrometry
Euro Mass Spectrometry 2018 (Italy) - Hyphenated Techniques
Euro Mass Spectrometry 2018 (Italy) - Ionization Techniques
Euro Mass Spectrometry 2018 (Italy) - Maintenance, Troubleshooting, Data Analysis and Experimentation in Mass Spectrometry
Euro Mass Spectrometry 2018 (Italy) - Mass spectrometry imaging
Euro Mass Spectrometry 2018 (Italy) - Mass Spectrometry in Proteome Research
Euro Mass Spectrometry 2018 (Italy) - New Approaches in Mass Spectrometry
Euro Mass Spectrometry 2018 (Italy) - Proteomics and its applications
Euro Mass Spectrometry 2018 (Italy) - Recent Advances and Development in Mass Spectrometry
Euro Mass Spectrometry 2018 (Italy) - Spectroscopy
Euro Mass Spectrometry 2018 (Italy) - Track 9: Proteomics from Discovery to Function and its applications
Euro Mass Spectrometry 2018 (Italy)
Peer Reviewed Journals
Journals by Subject
Clinical & Medical Journals
International Conferences 2018-19
