Friday, 31 July 2020

ENTREPRENEURSHIP SESSION 5 HAND OUT: IMPLEMENTATION OF THE DEVELOPMENT VISION 2025

The implementation of the Development Vision 2025 should fundamentally embody the following attributes: 

  Developmental mindset and competitiveness

  In order for the Tanzania society to attain this level, there is need to:

Ensure existence of sound economic management Increasingly promote investment in infrastructure by involving government, private sector and various communities of the society.

Reactivate the commitment to self-reliance, and re-cultivate resourcefulness and savings culture in order to curb and overcome the donor dependency syndrome which has led many Tanzanians into unprecedented apathy; Transform the education system so that it can develop the human capital in tandem with the socio-economic changes envisaged in the Vision 2025. The curriculum at various levels of education should be overhauled alongside the needs of implementing the vision 2025 

 Democratisation and popular Participation

  In order for the Tanzania Society to reach this level, there is a need to:   Create an open and democratic society that provides equal opportunity to every person. This entails creation of an active and participatory civil society in the articulation of its needs and in taking pride to fulfill its societal responsibilities;

  Sensitize society to use the democratic election mechanism at its disposal to elect good incorruptible and responsible leaders. Leaders with personal integrity, committed to the development of society and to the pursuit of the interests and welfare of the whole society; Improve public service delivery by ensuring that public servants are accountable to the people; 

Permit a greater role for local actors to own and drive the process of their development. Local people know their problems best and are better placed to judge what they need, what is possible to achieve and how it can effectively be achieved.

Decentralize the political administration and the fiscal structure roles and responsibilities on the basis of the principle of subsidiarity to commit individuals, households, communities and local government to the pursuit of the common Vision goal; 

Monitoring, Evaluation and Review 

This framework is essential in order to:

  Ensure that the process of evaluation and monitoring is used to track down progress towards the realization of the Development Vision goals. The best way to track down such progress is to start with ~ The envisioned end-result and work backwards to map out the milestones;Develop specific performance benchmarks and measurable outputs to assist in monitoring the process of implementing the Development Vision goals; 

Review the Development Vision in every five years so to gauge how the nation is faring and what adjustments need to be made as part of a regular evaluation and monitoring exercise.   Establish an efficient system of information and communication to facilitate timely monitoring and evaluation and ensuring a synergy between the various actors in society.  

Governance and the Rule of Law 

  Existence of this framework requires the society to:

Build the capacity of the public sector, civil society, media, parliament, the law enforcement institutions and others inside and outside the government as a means to build accountability to concerns public; 

Sensitize the people and raise their level of awareness as necessitated by the need to implement the Development Vision;

  Adopt strategies to build integrity by promoting accountability and transparency.

  Ensure that all service delivering institutions provide correct information and analysis in response to their obligations to society; 

Enshrine and entrench the pillars and core values of the Development Vision into the Union Constitution to make them sacrosanct and thereby galvanizing Tanzanians behind their practical realization

Tuesday, 28 July 2020

LAWS AND ETHICS SESSION 6-13 DISCUSSION QUESTIONS.

1. Define

(a) Professional misconduct

(b) Breaches

(c) Pharmacy practice

2. A pharmaceutical personnel must have regard for human life what are the obligations of pharmaceutical personnel on.

(a) Induction or inhibition of gestation.

…………………………………………………………………………………………………………………………………………………..

(b)Growth, development and performance enhancer

…………………………………………………………………………………………………………………………………………………….

(c) Termination of life:

…………………………………………………………………………………………………………………………………………………...

3.  A pharmaceutical personnel must ensure access to essential medicine. Mention five (5) obligation

..................................................................................................................................................

4. A pharmaceutical personnel should ensure availability of safe, efficacious and quality medicines. Mention five (a) obligations of the pharmaceutical personnel.

..................................................................................................................................................

5 (a) Mention code of ethics number five

       ……………………………………………………………………………………………………….

   (b) Mention (four) 4 obligation of pharmaceutical personnel on code of ethics number 9.

        …………………………………………………………………………………………………………………………..

6. Mention medicines and medical supplies provided at a dispensary level.

     ………………………………………………………………………………………………….…………………………

7. Section 36 of the pharmacy act no. 1 of 2011 is about application for Permits. Describe it

       ………………………………………………………………………………………………………………………………………………………

8.   (a) Define unfit medicine and cosmetic products

       ………………………………………………………………………………………………………………………………………………………

      (b)Describe the procedures for handling of unfit medicine and cosmetics products at facility level

      ……………………………………………………………………………………………………………………………………………………………..

9. Mention Minimum important information in the Register book:

   ……………………………………………………………………………………………………………………………….

10. Mention Minimum important information in Application Form for Disposal of unfit and cosmetics products.

   ………………………………………………………………………………………………………………………………………………………..

11.  Draw a format of Annex 1

………………………………………………………………………………………………………………………………..

12. What are the names of the following forms?

     Annex I   ………………………………………………………………………………………

    Annex II   ………………………………………………………………………………………

    Annex III ……………………………………………………………………………………..

    Annex IV   ………………………………………………………………………………………

13. What is inspection checklist forms?

        ……………………………………………………………………………………………

14. Define sorting of unfit medicines and cosmetic products.

     …………………………………………………………………………………………………………………………………

15. Complete the table bellow

S/N

Categories

Disposal methods

1.

Solids, semi-solids and

Powders

2.

Liquids

3.

Antineoplastics

4.

Treated waste and landfill, high

temperature incineration

5.

Landfill without waste inertization

6.

Disinfectants

7.

PVC plastics, glass

(ampoules, bottles and

vials)

8.

Recycle, burn, landfill

16. Describe the procedures for sorting of unfit medicine and cosmetics products

      …………………………………………………………………………………………………………………………………………………………

 17. Verification process shall involve the following stages. Mention

          ……………………………………………………………………………………………………………………………………………………

 18. Describe Verification Exercise of Unfit Medicines and Cosmetic Products.

          …………………………………………………………………………………………………………………………………………………….

 19.  Create a Model of Verification Form of unfit medicine and cosmetics products

          ……………………………………………………………………………………………………………………………………………………

 20. Where do members/Participants of destruction of unfit medicine and cosmetics products are chosen from. Mention?

              …………………………………………………………………………………………………………………………………….

   21. Mention members/Participants involved in destruction of unfit medicine and cosmetics products

           …………………………………………………………………………………………………………………………………………………….

    22. Describe the procedures for destruction of unfit medicine and cosmetics products.

        …………………………………………………………………………………………………………………………………………..

     23. What is the Certificate of Destruction of Unfit Medicines and Cosmetic Products?

 

        

 


Friday, 17 July 2020

LAWS AND ETHICS SELF EVALUATION QUESTIONS


CHOOSE MOST CORRECT ANSWER

Destruction of unfit medicine and cosmetic products
    A. It is the responsibility of the Tanzania Food and Drug Authority (TFDA)
    B. It is the responsibility of the Tanzania Medical device and Drug Authority (TMDA)
    C. It is the responsibility of BRELA
    D. It is the responsibility of the Medical Store Department (MSD)
    E. It is the responsibility of the Tanzania Beaural of Standard (TBS)

During destruction of unfit medicine and cosmetic products A local task force or advisory committee should be established at an early. how many members does this committee have?
   A. 1
   B. 2
   C.3
   D.4
   E.5
During destruction of unfit medicine and cosmetic products Members/supervisors/participants are chosen from?
   A. The regulatory authority
   B. the ministry of local authority 
   c. the port authority
    D.The institution
    E.The Drug regulatory authority

Monday, 13 July 2020

LAWS AND ETHICS SESSION 12 SELF EVALUATION QUESTIONS


Describe the procedures for verification of Unfit Medicines and Cosmetic Products
..................................................................................................................................

Mention/List the procedures for verification of Unfit Medicines and Cosmetic Products
 ............................................................................................................................................

(a)What does sorting of unfit medicines and cosmetic products mean?
(b)Describe Verification Exercise of Unfit Medicines and Cosmetic Products
.............................................................................................................................................


LAWS AND ETHICS SESSION 10 AND 11 ASSIGNMENT QUESTIONS


Define 
Storage?
Good Storage Practices?
Distribution?
Good distribution practices?
Mention sections in the Pharmacy act relate to storage of medicines and medical supplies?
...........................................................
.........................................................
..........................................................
(a)As per pharmacy act no. 1 of 2011 what is section 44 states?
(b) Describe section 44 as per pharmacy act no 1 of 2011 

(a) Define unfit medicine and cosmetic products
(b) Describe procedures for handling of unfit medicines and cosmetics products at facility level




 A drug, medical device or herbal drug shall be deemed to be counterfeit if -
   A. ................. it is manufactured under a name which belongs to another drug medical device or herbal drug 
  B...............  it is an imitation of another drug or medical device or herbal drug 
   C. ..............  is a substitute for another drug  or medical device or herbal drug 
   D..............  it is manufactured under a name which belongs to the same drug medical device or herbal drug 
 c...............  it is not  imitation of another drug or medical device or herbal drug 

Define 
substandard medicine and cosmetics products
adulterated medicine and cosmetics products
expired medicine and cosmetics products
counterfeit medicine and cosmetics products
Any person who intends to dispose off unfit medicines or cosmetic products shall adhere to the following procedures: mention 
..................................................................
..................................................................
...............................................................
................................................................
Describe  Procedures for Application to Dispose off Unfit Medicines and Cosmetic products
.......................................................................................................................................................
(a) Define unfit medicines and cosmetics products
(b) Describe the procedures for Application to Dispose off Unfit Medicines and Cosmetic products      

 Draw a well labelled Annex I Format of Register Book
Prohibited drugs means any drug declared to be a prohibited drug in terms of the provisions of section 81 of the TFDA Act. Describe

MATOKEO YA AWALI ENTERPRENEURSHIP LEVEL 6-2. KUNA AMBAO KATI ONE ITARUDI ILE YA MWANZO.

TABORA POLYTECHNIC COLLEGE PHARMACEUTICAL SCIENCES DEPARTMENT EXAMINATION NUMBER  NTA LEVEL 6...