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  2. Forced free trial - Wikipedia

    en.wikipedia.org/wiki/Forced_Free_Trial

    A forced free trial is a direct-marketing technique, usually for goods sold by regular subscription, in which potential buyers are sent a number of free product sample, usually periodic publications. Often, publishers distribute free copies and the reader is not asked to subscribe.

  3. All-America Selections - Wikipedia

    en.wikipedia.org/wiki/All-America_Selections

    The plants are then tested at more than 40 independent sites located in 24 US states and 5 Canadian provinces. A test site is called a trial garden or trial ground. Each trial ground has at least one official AAS judge. The judge supervises the trial and evaluates entries for AAS at no charge. None of the judges are paid for their AAS activities.

  4. Park Seed Company Gardens - Wikipedia

    en.wikipedia.org/wiki/Park_Seed_Company_Gardens

    Park Seed's trial garden is part of the prestigious All-America Selections (AAS) program. Park Seed Company has been very active with AAS since the mid-1950s. Park Seed staff horticultural experts frequently serve as AAS judges, and five Park Seed executives have served as AAS president. The trial gardens and on-site retail store closed in 2013.

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    Download System Mechanic to help repair and speed up your slow PC. Try it free* for 30 days now.

  8. Seeding trial - Wikipedia

    en.wikipedia.org/wiki/Seeding_trial

    A seeding trial or marketing trial is a form of marketing, conducted in the name of research, designed to target product sampling towards selected consumers. In the marketing research field, seeding is the process of allocating marketing to specific customers, or groups of customers, in order to stimulate the internal dynamics of the market, and enhance the diffusion process.

  9. Biologics license application - Wikipedia

    en.wikipedia.org/wiki/Biologics_License_Application

    If the Form 356h is missing information, the FDA will reply within 74 days. [3] A BLA asserts that the product is "safe, pure, and potent", the manufacturing facilities are inspectable, and each package of the product bears the license number. Statutory standards for BLA approval are largely the same as those for New Drug Application approval.