Pharmacovigilance
The foundation of our brand and service lies in catering to the needs and safety of the patient, first. We enable end patients by setting up systems of communication and accountability like side-effect reporting and our pharmacovigilance watch department, advocating always for information dissemination and transparency in the market. Asterisk is empowered with all the qualifications necessary to meet global pharmacovigilance standards. Our Europe and US based pharmaceutical affiliates are equipped, to adhere to EU compliance requirements. All of our partner facilities have passed global regulatory inspections across 64 countries.
Asterisk’s methodical and thorough pharmacovigilance practices ensure that we are able to process and manage complaints and queries from multiple stakeholders – right from the end consumer to our affiliate partners and wholesalers. Our efforts towards greater transparency in pharmacovigilance involves us thoroughly understanding the role of our patients, wholesalers, healthcare practitioners and providers, affiliate partners, and regulatory bodies. We do this by regularly monitoring incoming data on the benefits, risks, and side-effects of each and every product we are responsible for.
Report a side effect
As a healthcare company, one of the responsibilities that we take complete ownership of is to ensure that patients consuming our products are safe. Our dedication to safety in medicine begins right from our research to end delivery through the supply chain process, across the world.
Any and all side effects should be discussed with your healthcare practitioner.
You may report an adverse event related to our products here:
By reporting a side effect, you hereby agree and consent that Asterisk Lifesciences Ltd. may collect, use, disclose and process your personal data submitted in this form and/or otherwise provided by you to us (i) in accordance with applicable laws and our Cookies and Privacy Policy and (ii) for the purposes of complying with the obligation under applicable laws to monitor the safety of medicines and for responding to medical information queries.
By submitting the form above, you also expressly consent to the transfer of your personal data (including but not limited to sensitive personal data) and the processing of such data outside the European Economic Area (“EEA”), including but not limited to Asterisk Lifesciences Ltd and other group members and their respective processors located in India or elsewhere. To check our group members please click here. While some group members are located in countries (such as India) with laws that (according to the European Commission) do not offer the same level of protection to personal data as that granted by EEA countries, Asterisk Lifesciences Ltd. and its group members do adopt reasonable state of the art security measures to prevent unauthorized and unlawful use of personal data.
At any time and subject to applicable laws, you may exercise the rights of access, rectification, cancellation, opposition and revoke your consent to use, disclose, transfer and process of your personal data, by contacting our data protection officer at abc@asterisk.com
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