Weston United Group! the world’s most predominant organization in delivering and discovering the latest research innovations in all fields to every corner of the globe. Our utmost enhanced and modernized smart platform, upholds the high standard top-quality conferences at various multicultural international venues and medical services throughout the year. Our collaboration with MDPI publishers, various international universities, organizations and research centers build a vast networking globally and sprout a creative approach in finding research inventions.
We are continuously dedicated and uncompromised in bridging social gaps and showcasing future breakthroughs, thereby becoming the most significant pioneers of the world. We rather stream into all sectors of the academia emphasizing mainly into technology and scientific arenas. With over 1000+ subscribers, 550+ collaborators and 60+ country participants we are gratified in organizing the best international conferences all over the world.
Our VISION is to liquify the gaps of research knowledge and uncover innovations to strengthen all the communities of mankind globally. Weston United Group is mainly aimed at flawless networking of all professionals in a particular field and spur their academia to greater heights all over the world.
Our success comes from the minds of people. We construct the conference platform from the perspective of attendee thinking and mingle with ongoing market research, therefore exploring the remarkable and valuable research findings for the delegates who are attending our conferences. We are proud to say that our unique concept in conducting conferences brings you worthful benefits and heartful satisfaction for our global attendees.
Our MISSION is to help millions of scientists, doctorates, professionals and students to access new research outcomes in their respective field and sharpen themselves to dispense knowledge for next generations.
We organize a wide array of top international conferences throughout the year covering all streams of Engineering, Medical, Technology, Arts and Business professions. Our years of proficiency and expertise in this field is a launchpad in steering distinct workshops, symposiums, special sessions, B2B meetings, panel discussions and exhibitions to all academic and business professionals.
We are seamlessly committed to gather world renowned scientists, global eminent industry experts in all streams of events, where you can create and exchange your research ideas, discuss thoughts, meet your peers face to face and magnify professional networking for your career growth globally. Undoubtedly, this is the platform which gives you a great knowledge with intense research discussions and reach your expectations with our high-quality budget friendly conferences every year.
Be the first of all to hear about the latest developments, discover stimulating case studies and future global research discoveries in all subjects on our unique Weston Conferences podium.
we also stepped into various medical and clinical services to explore the knowledge into healthcare sector and provide phenomenal facilities for our clients.
The stringent regulations on safety monitoring and their periodical revision have led to increased safety data collection, analysis and regulatory surveillance, and increased costs. Thus, Pharmacovigilance has become a critical phase in clinical development programs.
Our Pharmacovigilance Services help you ensure regulatory compliance, enhance efficiency and reduce costs significantly. We are offering the service of CRO in India that operate within a partnership model, where you benefit from our domain knowledge, quality systems approach, multi-disciplinary safety expertise and adherence to reporting timelines of the EMEA, FDA, MHRA and other competent authorities.
We offer Pharmacovigilance Services, which include data collection, processing, medical review, safety writing, report writing, reporting, signal detection and analysis.
We provide comprehensive solutions across all phases of clinical development and post-marketing to pharmaceutical, biotechnology and medical device companies. The dedicated Pharmacovigilance team comprises of Clinical Pharmacologists with in-depth knowledge in diverse therapeutic areas and several years of Pharmacovigilance and safety project management services experience. The complete range of high-quality services offered by the Pharmacovigilance team encompasses:
Our Services Include:
• Literature search in compliance with regulatory requirements.
• Collection, evaluation, analysis and reporting of safety information from all sources including spontaneous reports of adverse events of the marketed drugs.
• Online coding (MedDRA, WHO DDE) of Adverse Events.
• Medical review of case reports.
• Preparation of safety narratives.
• Preparation and submission of Periodic Safety Update Reports (PSURs) to regulatory authorities.
• Preparation and submission of expedited reports to regulatory authorities.
We are one of the prominent Pharmacovigilance companies in India that deliver services within time and budget, further assist in lowering the overall cost base for drug safety activities that is ensured through focus on short lead-in times, clear and concise processes tailor made to meet client expectations ultimately leading to effective client management and their satisfaction.
MEDICAL WRITING SERVICES
Medical Writing team provides ICH GCP compliant clinical trial documents, accurately written documents as per standard formats, medical writing services ranging from entire drug development life cycle, and to the post-marketing reporting and commercialization writing. Our team of medical writers delivers accurate, timely, and cost-effective clinical and regulatory documents to the highest quality and scientific standards. Our medical writers are very flexible to meet your needs, using our expertise to transform your complex and diverse data into an accurate and evidence-based clinical profile of the drug concerning treatment/patient safety.
Our Services Include:
• Preparation of ICH GCP compliant Clinical Trial documents (Protocol development, Informed Consent Forms, Investigator Brochures, Patient Narratives, and Clinical Study Reports).
• Labeling Documents (Patient Information Leaflets, Labelling Updates, Core Data Sheet (CDS) and Package Inserts).
• Publications (Copywriting, Copyediting, Proofreading, Journal Articles, Manuscripts, Abstracts, Posters, and Presentations).
• Pharmacovigilance; Periodic Safety Update Reports (PSUR), Periodic Benefit Risk Evaluation Report (PBRER), Preparation and Review of Annual Safety Reports (ASRs), Development Safety Update Reports (DSUR), Periodic Adverse Drug Experience Reports (PADER).
• Medical marketing reviews and reports
• Literature search and reviews
• Publication planning
• Scientific manuscripts
• Safety Narratives
Our unique program concepts that sets us apart from the rest
We prioritize discussions on talks to understand the concepts clearly and apply to your academics and research projects.
Get recognized and connected globally by showcasing your research projects and boost support for your future discoveries.
We are driven with quality and committed for regulatory pharmacovigilance services.
We have panel of experts in delivering quality of writing services.
We double check the data to adhere regulatory guidelines.
We also provide all types of content writing services including the web content.