Questions

Glycogen is the storage form of glucose in animals and humans which is analogous to the starch in plants. Glycogen is synthesized and stored mainly in the liver and the muscles.

Convection is the mode of heat transfer which involves bulk motion of a fluid to transfer heat. Energy transfer by convection is primarily restricted to fluids. Fluids can be both liquids and gases.

The Integrative Project Management Processes include:

Develop Project Charter - Developing the project charter that formally authorizes a project or a project Phase.

Develope Preliminary Project Scope Statement - Developing the preliminary project scope statement that provides a high level scope narrative

Develop Project Management Plan -  Documenting the actions necessary to define, prepare, integrate, and coordinate all subsidiary plans into a project management plan.

Direct and Manage Project Execution- Executing the work defined in the project management plan to achieve the project's requirements defined in the project scope statement.

Monitor and Control Project Work - Monitoring and controlling the processes used to initiate, plan, execute, and close a project to meet the performance objectives defined in the project management plan.

Integrated Change Control - Reviewing all change requests, approving changes, and controlling changes to the deliverables and organizational process assets.

Close Project - Finalizing all activities across all of the Project Management Process Groups to formally close the project or a Project phase.

The relationship where both the participating entities belong to same entity type is called Recursive relationship

24 hours

Bureau of Pharma PSUs of India (BPPI) is the implementing agency of Pradhan Mantri Janaushadhi Pariyojana (PMBJP). BPPI was established in December2008 under the Department of Pharmaceuticals, Government of India. The Bureau has been registered as an independent society under the Societies RegistrationAct, 1860 as a separate independent legal entity in April, 2010. BPPI follows the provisions of GFR, 2017 as amended from time to time, the CVC guidelines, and instructions from the Department of Pharmaceuticals.