Evaluation of Consistency Quality

  • Check with publisher
  • Published date: May 23, 2019
    • Shirley, New York, United States

A generic drug is the formulation that has the same performance as an innovator product, including same dosage, effectiveness, dosage form, strength, quality and other properties. The greatest advantage for a generic drug is far more economical compared to the Innovative ones. As an alternative form for the branded medicines, generic drugs have an increasing market share in recent years since they are safe and effective and of the same high quality. Taking the United States for example, the generic copy has accounted for 69% of all prescriptions dispensed and the dollars spent on prescriptions only accounted for 16% of all budget.

With knowing the strong aspiration to produce high quality pharmaceutical products, the generic medicine experts at BOC Sciences have enough professional knowledge to help you determine the most optimal formulation to ensure the generic ones are made to the same standard as branded medicines. Moreover, through identification of the most critical needs of patients across the globe and the potential profit margin, our strategist will assist you to select the most valuable program to maximize the benefits.


Result 0 votes
Alex Brown
0 votes

Useful information

  • Avoid scams by acting locally or paying with PayPal
  • Never pay with Western Union, Moneygram or other anonymous payment services
  • Don't buy or sell outside of your country. Don't accept cashier cheques from outside your country
  • This site is never involved in any transaction, and does not handle payments, shipping, guarantee transactions, provide escrow services, or offer "buyer protection" or "seller certification"

Related listings

  • Generics Consistency Evaluation

    Generics Consistency Evaluation

    Drug Development Shirley (New York) May 23, 2019 Check with publisher

    The generic consistency evaluation is composed by quality conformance and efficiency consistency. Evaluation of pharmaceutical quality conformance is defined to determine whether your generic drug preparation and reference formulations are consistent...

  • Registration and Submission

    Registration and Submission

    Drug Development Shirley (New York) May 23, 2019 Check with publisher

    The so-called drug registration and submission represents that the state food and drug administration (FDA), in accordance with the application of the drug registration applicant, makes a systematic evaluation of the safety, effectiveness and quality...

  • in vitro- in vivo correlations (IVIVC)

    in vitro- in vivo correlations (IVIVC)

    Drug Development Shirley (New York) May 23, 2019 Check with publisher

    During the total process of drug development, formulation optimization represents a critical aspect to ensure the quality of pharmaceutical products. However, the formulation optimization is always a complex and time consuming procedure that generall...