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"Understanding Pharmaceutical Medicines: Your Guide to Treatment"ntitled

<br>Pharmaceutical medicine is what doctors prescribe to help people feel better when they're sick. It comes in different forms like pills, liquids, or injections. These medicines are made by experts called pharmacists and scientists who carefully study how they work. They're designed to treat specific health problems, like infections, pain, or allergies. Remember to always follow the instructions on the label and talk to your doctor if you have any questions.<br><br><br><br>

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"Understanding Pharmaceutical Medicines: Your Guide to Treatment"ntitled

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  1. Introduction to Pharmaceutical Medicine Pharmaceutical medicine encompasses the study, research, and development of medications. It involves interdisciplinary approaches to ensure the safety and effectiveness of pharmaceutical products. by Roshni Mahato

  2. Drug Discovery and Development Process Research & Analysis Testing & Optimization Regulatory Considerations Scientists identify potential compounds and assess their properties for therapeutic use. Candidates undergo rigorous testing and optimization to enhance efficacy and safety. Understanding and adhering to regulations play a pivotal role in this stage.

  3. Preclinical Studies 1 2 Animal Models In Vitro Testing Preclinical studies utilize animal models to assess efficacy and safety. Pharmacokinetics and toxicology are evaluated in controlled laboratory environments. 3 Data Collection Comprehensive data collection and analysis is a critical aspect of preclinical studies.

  4. Clinical Trials 1 Phase I Initial testing for safety, dosage, and potential side effects in small groups. 2 Phase II Evaluating efficacy and side effects in a larger group of patients. 3 Phase III Large-scale testing for final assessment of safety and efficacy.

  5. Regulatory Approval Process Submission Review & Analysis Approval Application submission to regulatory authorities for approval. Rigorous review process to assess safety, efficacy, and quality. Final decision on market approval and conditions for use.

  6. Post-Marketing Surveillance Adverse Events Monitoring Risk Assessment Ongoing monitoring of adverse reactions after a drug reaches the market. Assessing potential risks and benefits in a real-world setting. Regulatory Compliance Ensuring compliance with pharmacovigilance and reporting regulations.

  7. Pharmacovigilance Data Analysis Adverse Event Reporting Global Vigilance Utilizing advanced technology for comprehensive data analysis. International collaboration and vigilance for pharmaceutical products. Efficient reporting and assessment of potential adverse events.

  8. Future of Pharmaceutical Medicine AI Integration Telemedicine Biotechnology Advancements AI Integration Telemedicine Expansion Biotechnology Advancements Integration of advanced AI for drug discovery and personalized medicine. Enhanced use of telemedicine for diagnosis, treatment, and monitoring. Emerging biotechnological advancements for improved therapeutics.

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