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2. Zazzle - Wikipedia

   en.wikipedia.org/wiki/Zazzle

   Zazzle. Zazzle is an American online marketplace that allows designers and customers to create their own products with independent manufacturers (clothing, posters, etc.), as well as use images from participating companies. Zazzle has partnered with many brands to amass a collection of digital images from companies like Disney, Warner Brothers ...

3. Clinical Trials Registry – India - Wikipedia

   en.wikipedia.org/wiki/Clinical_Trials_Registry...

   Clinical Trials Registry – India ( CTRI) is the government of India's official clinical trial registry. The National Institute of Medical Statistics of the Indian Council of Medical Research established the CTRI on 20 July 2007. [1] Since 2009 the Central Drugs Standard Control Organisation has mandated that anyone conducting clinical trials ...

4. Pivotal trial - Wikipedia

   en.wikipedia.org/wiki/Pivotal_trial

   Pivotal trial. A pivotal trial is typically a Phase III clinical trial in the multi-year process of clinical research intended to demonstrate and confirm the safety and efficacy of a treatment – such as a drug candidate, medical device or clinical diagnostic procedure – and to estimate the incidence of common adverse effects. [1]

5. Zazzle | TechCrunch

   techcrunch.com/tag/zazzle

   The creator economy loves merch, which is great news for on-demand custom printing startups such as Latvia-based Printify — today it’s announcing a $45 million Series A round, led by…

6. Apple offers a free one-month trial of MLS Season ... - Engadget

   www.engadget.com/apple-offers-a-free-one-month...

   Apple has begun offering a free one-month trial for MLS Season Pass.The promotion is available in every country where you can sign up for the streaming package, and both new and returning monthly ...

7. Common Technical Document - Wikipedia

   en.wikipedia.org/wiki/Common_Technical_Document

   The CTD is an internationally agreed format for the preparation of applications regarding new drugs intended to be submitted to regional regulatory authorities in participating countries. It was developed by the European Medicines Agency (EMA, Europe), the Food and Drug Administration and the Ministry of Health, Labour and Welfare (Japan ...