Welcome to Pharmcontrol Experts in Pharmacovigilance and Regulatory Affairs Services in Azerbaijan
Pharmcontrol is a leading provider of pharmacovigilance services and drug registration solutions for pharmaceutical, medical device, and cosmetic companies worldwide. We support businesses in over 30 countries, including the United Kingdom, Germany, Turkey, India, China, the United States, and across Eastern Europe and Central Asia. Our pharmacovigilance service ensures full compliance with global safety standards, offering expert monitoring, risk management, and regulatory guidance. Whether you’re launching a product or managing an existing portfolio, Pharmcontrol delivers reliable, high-quality support tailored to your market.
Pharmacovigilance: A Key Role in Ensuring Drug Safety
– Pharmacovigilance Systems: We develop and implement effective pharmacovigilance systems tailored to Azerbaijani regulatory requirements.
– Pharmacovigilance in Medical Institutions: Ensuring drug safety and patient care is critical in Azerbaijan’s medical landscape.
– Pharmacovigilance Reporting: We ensure complete and timely pharmacovigilance reporting in compliance with Azerbaijani legislative requirements.
– Pharmacovigilance for Medical Devices: Our services extend to pharmacovigilance for medical devices and dietary supplements in Azerbaijan.
– New Pharmacovigilance Requirements: We stay updated on local requirements and standards, ensuring compliance in Azerbaijan.
– Pharmacovigilance Vacancies: Pharmcontrol offers career opportunities for pharmacovigilance specialists and those involved in the authorization of medicines in Azerbaijan.
Pharmacovigilance Worldwide
Pharmacovigilance plays a crucial global role in medicine by ensuring drug safety and efficacy. Our experts are well-versed in international legislation, providing professional support for pharmacovigilance processes worldwide.
Defining Pharmacovigilance and Its Objectives
What is Pharmacovigilance?
Pharmacovigilance involves the systematic monitoring of the safety and effectiveness of medicines before and after market release. Key tasks include:
– Assessing drug safety.
– Monitoring adverse drug reactions.
– Conducting clinical research.
– Developing and implementing pharmacovigilance systems in healthcare organizations.
– Analyzing and reporting pharmacovigilance data.
Pharmacovigilance and Drug Quality
Pharmacovigilance aims to ensure high-quality pharmaceutical products through quality control, audits, and staff training on risk management approaches.
Electronic Pharmacovigilance
As technology evolves, electronic pharmacovigilance becomes increasingly relevant.
Professional Partnership
We collaborate with leading global organizations and institutions in international projects, keeping abreast of new pharmacovigilance requirements and standards.
Pharmacovigilance Outsourcing Company:
We offer outsourcing services in pharmacovigilance to enhance efficiency and reduce costs for Azerbaijani companies.
Contact Information
For more details about our services and pharmacovigilance vacancies in Azerbaijan, contact us at info@pharmcontrol.az.
Report an Adverse Reaction
To report an adverse drug reaction, please use our form. Your feedback is crucial in ensuring patient safety.
Don’t delay your pharmacovigilance concerns. Contact us today to ensure the safety and successful market launch of your pharmaceutical and cosmetic products in Azerbaijan.
How does the safety of medicines work?
Treatment
Recognise
Report
Collect
Analyse
Act
Communicate
Prevent
How does the safety of medicines work?
Prevent
Communicate
Act
Analyse
Collect
Report
Recognise
Treatment
Pharmacovigilance is a system for monitoring the safety of medicines, medical devices, vaccines and other products in the health sector, which is aimed to protect patients from potential harm. The purpose of pharmacovigilance is to ensure the safety, quality, and effectiveness of medical products in order to protect public health. Pharmacovigilance involves the constant monitoring of data on side-effects and reactions to medicinal products. Every person at various stages of their life takes medicines and deals with side-effects. This highlights the importance of the pharmacovigilance system. Let’s examine Mike’s story to understand how the medication safety process works.
This is Mike
He is 48 years old and he had been diagnosed with arterial hypertension. The latest results of his tests show that his blood pressure is no longer controlled by the medication that he is taking.
Treatment
Mike visits the doctor, who prescribes him a new medication, “Genpress”. Mike acquires the medication at the pharmacy, where the pharmacist informs him about the possible side-effects: fatigue, dizziness, and dryness in the mouth. After a week, Mike starts experiencing shortness of breath and a feeling of tiredness, and a few days later, he notices that his heartbeat is becoming irregular.
Recognise
Mike’s doctor does blood tests and an electrocardiogram, which confirm the doctor’s suspicion that Mike has developed arrhythmia. The doctor advises Mike to stop taking “Genpress”medicine. Over the next two weeks, Mike no longer experiences shortness of breath or fatigue, and his heartbeat stabilizes.
Report
Mike’s doctor, carrying out her responsibilities on pharmacovigilance, analyzes the report on the side effect experienced by Mike after taking the medicine. She uses pharmacovigilance information systems to confirm her suspicions and fill out report of an adverse event for submission to the regulatory authority.
Collect
After the medication is registered, the practice of pharmacovigilance begins, which includes the collection and analysis of information about potential side- effects.
Analyse
Researches in the field of pharmacovigilance shows that, the medicine can cause serious complications. For instance, an analysis by a national regulatory authority found that “Genpress” caused Mike’s arrhythmia.
Act
Authorized body on pharmacovigilance decides that, the manufacturer must make changes to the labeling, including arrhythmia in the “Side Effects” section and the potential risk of serious heart issues in the “Warnings” section.
Communicate
The changes to the labeling can be distributed to healthcare providers in various ways. For example, doctors may receive an advisory letter with additional information available on the website of the national pharmacovigilance authority.
Prevent
Mike’s reports on side-effects helped to identify the risks of “Genpress” medicine. This is not only helps to uncover previously unknown side-effects, but also provides new knowledge of the ways to reduce side effects. Mike’s physician switched him to the medicine “Pipraten”, and no adverse reactions were observed. This is a classical case underscoring the crucial role of pharmacovigilance.
Pharmacovigilance is a system for monitoring the safety of medicines, medical devices, vaccines and other products in the health sector, which is aimed to protect patients from potential harm. The purpose of pharmacovigilance is to ensure the safety, quality, and effectiveness of medical products in order to protect public health. Pharmacovigilance involves the constant monitoring of data on side-effects and reactions to medicinal products. Every person at various stages of their life takes medicines and deals with side-effects. This highlights the importance of the pharmacovigilance system. Let’s examine Mike’s story to understand how the medication safety process works.
This is Mike
He is 48 years old and he had been diagnosed with arterial hypertension. The latest results of his tests show that his blood pressure is no longer controlled by the medication that he is taking.
Treatment
Mike visits the doctor, who prescribes him a new medication, “Genpress”. Mike acquires the medication at the pharmacy, where the pharmacist informs him about the possible side-effects: fatigue, dizziness, and dryness in the mouth. After a week, Mike starts experiencing shortness of breath and a feeling of tiredness, and a few days later, he notices that his heartbeat is becoming irregular.
Recognise
Mike’s doctor does blood tests and an electrocardiogram, which confirm the doctor’s suspicion that Mike has developed arrhythmia. The doctor advises Mike to stop taking “Genpress”medicine. Over the next two weeks, Mike no longer experiences shortness of breath or fatigue, and his heartbeat stabilizes.
Report
Mike’s doctor, carrying out her responsibilities on pharmacovigilance, analyzes the report on the side effect experienced by Mike after taking the medicine. She uses pharmacovigilance information systems to confirm her suspicions and fill out report of an adverse event for submission to the regulatory authority.
Collect
After the medication is registered, the practice of pharmacovigilance begins, which includes the collection and analysis of information about potential side- effects.
Analyse
Researches in the field of pharmacovigilance shows that, the medicine can cause serious complications. For instance, an analysis by a national regulatory authority found that “Genpress” caused Mike’s arrhythmia.
Act
Authorized body on pharmacovigilance decides that, the manufacturer must make changes to the labeling, including arrhythmia in the “Side Effects” section and the potential risk of serious heart issues in the “Warnings” section.
Communicate
The changes to the labeling can be distributed to healthcare providers in various ways. For example, doctors may receive an advisory letter with additional information available on the website of the national pharmacovigilance authority.
Prevent
Mike’s reports on side-effects helped to identify the risks of “Genpress” medicine. This is not only helps to uncover previously unknown side-effects, but also provides new knowledge of the ways to reduce side effects. Mike’s physician switched him to the medicine “Pipraten”, and no adverse reactions were observed. This is a classical case underscoring the crucial role of pharmacovigilance.
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