In the global carbon cycle microorganisms have evolved a variety of methods for fixing carbon. Researchers from Bremen and Taiwan have investigated the methods that are utilized at extremely hot, acidic and sulfur-rich hydrothermal vents in shallow waters off the island of Kueishantao, Taiwan.
Antiseizure medication is usually prescribed for people with the condition. However, for one in three people with epilepsy around 20 million individuals worldwide, current antiseizure medications are ineffective. This means that people will continue to have seizures despite taking medication – a condition called ‘drug resistance.
As we age, blood stem cells, the essential source of new blood cells in the body, can accumulate genetic mutations. These mutations can give the cells a growth advantage, laying the foundation for developing serious health conditions. Now, scientists at The Jackson Laboratory (JAX) have not only discovered the mechanism that fuels their unchecked growth but have also found a way to stop it.
Professional having B.Pharm, BAMS, B-Tech, MPH. Preference will be given to professionals having experience in Digital Health. Foster partnerships with academia, industry, and international organization to accelerate digital health adoption.
Masters Degree in Chemistry, Pharmacy, Forensic Science specialization in Forensic Chemistry and Toxicology, Bio Chemistry from a recognized University. Assistant Director Chemistry and Toxicology, in Directorate of Forensic Services, Home Department
D.Pharm, Integrated Pharmacy Course for certificates issued by Government. vacant posts on a lump sum basis through the District Welfare Association on the basis of contract of the Siddha Medical Department.
To support the teaching needs of the M.Sc. in Clinical Research program with a specialization in Clinical Trials at THSTI.
Contribute ongoing and future clinical trials, epidemiological studies, and other health- related research projects by providing robust statistical expertise.
A Diploma in Pharmacy, Bachelor of Pharmacy. Must have registered with Pharmacy Council and must keep the registration alive by renewing it regularly every year.
BPharm, BSc, MPharm, MSc, MBBS, BAMS; Experience in PV/ Clinical Research drug safety preferred. Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code and enter data.
RM, PM, FG, Dispensing, Dispatch, Documentation. After a journey of growth spanning 27 years as Cadila Healthcare Ltd. and the Zydus Group, we have evolved and transformed ourselves in response to the changing times.
TCS combines tech expertise and business intelligence to catalyze change and deliver results. Our mission is to help customers achieve their business objectives by providing innovative, best-in-class consulting, IT solutions and services and to make it a joy for all stakeholders to work with us. Clinical Data, Regulatory, Clinical Operations, Pharmacovigilance; Should be open to work In shifts
Expertise in designing, executing, and reviewing cleaning validation protocols. ensuring compliance with cGMP. EMA. and other global regulatory requirements. Specializing in stability studies, regulatory compliance, and quality assurance oversight. Managing stability programs in alignment with ICH guidelines
As part of our team, you'll be responsible for a diverse range of tasks within the drug discovery process. In this role, you will have ample opportunities to collaborate with our dynamic team, providing scientific expertise and strategic leadership.
Hands-on experience with HPLC, GC, UV-Visible Spectroscopy and Dissolution tester. Proficient in Empower-3 software.
Strong analytical and problem- solving skills.
As Technical Leader, define, organize, plan and lead the projects that are technically complex and cross functional in nature at a global front. Broad understanding of the overall product and therapy along with deep technical expertise in one or more fields related to drugs and medical devices
The Clinical Data Management Associate is responsible for providing expert skills as part of the clinical data management team within the Data Management and Statistics Department to ensure that efficient and quality data management products are produced in accordance with customer requirements.
The Senior Specialist, Expert License Management prepare dossiers and execute actions that support the license security and product compliance on the markets, and that meet companys and health authorities requirements. Encounter the challenges to enable representatives from all major disciplines involved to reach agreement on the license management strategy and approach.
• Clinical Research (PGDCR/EDCR) • Pharmacovigilance (PGDPV/EDPV) • Pharmaceutical Regulatory Affairs (PGDPRA/EDPRA) • Pharmaceutical Quality Assurance and Quality Control (PGDPQAQC/EDPQAQC) • Big Data Analytics (PGDBDA/EDBDA) • Medical Device Management (PGDMDM/EDMDM) • Pharmaceutical Sciences (PGDPS/EDPS) • Pharmaceutical Business Analytics (PGDPBA/EDPBA) • Medical Coding (PGDMC/EDMC) • Good Manufacturing Practices (PGDGMP/EDGMP) • Food Science and Technology (PGDFST/EDFST) • Nanotechnology (PGDNT/EDNT) • Clinical Psychology (PGDCP/EDCP) • Public Health and Hospital Management (PGDPHHM/EDPHHM) • Intellectual Property Rights (PGDIPR/EDIPR) • Pharmaceutical Regulatory Affairs (PGDPRA/EDPRA) • Environmental Social & Governance (PGDESG/EDESG) • Environment Health and Safety (PGDEHS/EDEHS) • Environment Regulatory Affairs (PGDERA/EDERA) • Environmental Studies and Resources Management (PGDESRM/EDESRM) • Herbal Formulations (PGDHF/EDHF) • Cognitive Behavioural Therapy (CBT) • Neuropsychology (PGDNP/EDNP) • Integrative Medicine (PGDIM/EDIM) • Maternal and Child Health (PGDMHC/EDMHC) • Yoga Therapies (PGDYT/EDYT) • Ayurveda Practices (PGDAP/EDAP/DAP) • Public Health and Hospital Management (PGDPHHM/EDPHHM)
• Pharmaceutical Management (PGDPM/EDPM) • Pharmaceutical API Manufacturing (PGDPAM/EDPAM) • Pharmaceutical Formulation (PGDPF/EDPF) • Pharmaceutical Chemistry (PGDPC/EDPC) • Pharmaceutical Process Engineering (PGDPPE/EDPPE) • Herbal Drug Technology (PGDHDT/EDHDT) • Herbal Medicine (PGDHM/EDHM) • Bioinformatics (PGDBI/EDBI) • Pharmaceutical Packaging (PGDPP/EDPP) • Pharmaceutical Production (PGDPP/EDPP) • Computer Aided Drug Design (PGDCADD/EDCADD) • Computer System Validation (PGDCSV/EDCSV) • Regulatory Affairs (Medical Device as Major) (PGDRAMDM/EDRAMDM) • Biomedical Technology (PGDBT/EDBT) • Nanomedicine • Ayurvedic Cosmetology (PGDAC/EDAC) • Cosmetic Technology (PGDCT/EDCT) • Herbal Cosmetics (PGDHC/EDHC) • Dermacare Formulations (PGDDF/EDDF) • Clinical Nutrition (PGDCN/EDCN) • Sports and Fitness Nutrition (PGDSFN/EDSFN) • Nutrition and Dietetics (PGDND/EDND) • Obesity and Weight Management (PGDOWM/EDOWM) • Clinical Diabetology (PGDCD/EDCD) • Public Health Nutrition (PGDPHN/EDPHN) • Medical Nutrition Therapy (PGDMNT/EDMNT) • Pediatric Nutrition (PGDPN/EDPN)
Certificate Programmes:
• GMP for Pharmaceutical & Manufacturing Processes • Pharmaceutical GMP Auditor • Medical Device Quality Auditor • Drug Regulatory Affairs Professional • Good Laboratory Practice Professional (CGLPP) • Certified Sports Nutritionist • Certified Fitness Nutrition Specialist • Certified Diabetes Educator • FSMS Lead Auditor (5 Days Training) • FSSC 22000 Lead v6 Auditor (5 Days Training) • HACCP Level 4 Auditor (5 Days Training) • Food Regulatory Affairs Professional (5 Days) • Food Quality Manager (5 Days) • Food Quality Technician (5 Days) • Laboratory Management Systems (ISO/IEC 17025:2017) Lead Auditor Training (5 Days) • Certificate in Occupational Health and Safety Management Systems (OHSM) • Corporate Social Responsibility Compliance (CSRC) • Environmental Social & Governance (ESG) • Healthcare Waste Management
• Food Safety Management Systems (FSMS) (5 Days Training) • HACCP (3 Days Training) • BRC Global Standards for Food Safety and Quality (5 Days Training) • Food Packaging (5 Days) • Food Supply Chain Management (5 Days) • Good Manufacturing Practices (5 Days) • Food Sensory Analysis (5 Days) • Dairy Science and Technology (5 Days) • Cold Chain Management (5 Days) • Entrepreneurship Development in Food Industries (5 Days) (e.g., Bakery, Beverage, Milk Industry) • Food GMP Professional (5 Days) • Food Quality Auditor (5 Days) • FSMS Internal Auditor (5 Days Training) • Business Responsibility and Sustainability Report (BRSR) • Environmental Management Systems (ISO 14001:2015) Lead Auditor
✓ Programme duration: Programme duration: 12 months for Post Graduate Diploma, 6 months for Executive Diploma and 3 months for Professional Certification programmes.
✓ Contact for Prospectus and last date on: 18001031071 or info@igmpi.ac.in
Ph.D, MD, MS, MDS or equivalent degree or having 3 years of research experience after MVSc, M.Pharm, ME, M.Tech with at least one research paper in Science Citation Indexed journal.