Tourist visa allows 90-day stays in multiple entries for 1 year. Employment visa requires sponsorship and medical screening. Student visa available for citizens of over 160 countries
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CTD is an international standard for pharmaceutical registration applications. Developed in 2000 by EMA, FDA and Japanese Ministry of Health. Replaced regional-specific guidelines in 2002. Aims to reduce time and resources for regulatory submissions
Guide updated weekly with information from International Bureau. EPO headquarters located in Munich, with branches in The Hague and Berlin. Fax filing prohibited from July 2024 onwards. Electronic filing accepted via various EPO services
PMA must include applicant name, address, and separate sections for nonclinical and clinical studies. Summary section should be 10-15 pages long, providing general understanding of application. Device description, manufacturing process, and performance characteristics must be included. Marketing history and clinical study results must be summarized. Technical sections require detailed data on nonclinical and clinical studies