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Teesta River Agreement Between India And Bangladesh

A simplistic imposition of developing geopolitics in the region could not live up to the complexity of the complicated hydrodynamic relationship between the two neighbors, who share 54 rivers between them. Sayanangshu Modak is a junior fellow at ORF Kolkata. He works on the broad themes of transboundary water policy, hydrodiplomacy and flood risk management. Its current research centre is located at the intersection of science and policy for effective watershed governance. >> A general view of the Teesta River can be seen on September 8, 2011 in Sevok, about 20 km from Siliguri. Indian Prime Minister Manmohan`s visit to Bangladesh, on the 6th According to reports, Mamata Banerjee, India`s Prime Minister of West Bengal, has been tarnished by the uncertainty surrounding the signing of a Teesta River watershed agreement. AFP PHOTO/Diptendu DUTTA | Photo: AFP How do we measure the sharing of water from the river and if Bangladesh is looking for more water, why can`t India make the same claim? “If they want to keep the monsoon water in the river after dredging, they have to build a structure [like ponds, reservoirs and canals] in the downstream part of the Thesta. So before we make a comment, we need to know more about what they intend to build and how they are going to do it,” Nishat said. Bangladesh expressed “deep concern” about the increase in the number of deaths at the Indo-Bangladesh border by “BSF or Indian nationals” in the first half of this year, and the Indian side assured that the BSF authorities have been sensitized to this issue during the DG-level discussions between bangladeshi border guards and BSF to be held next month in Dhaka, this should be discussed in detail. After coming to power in 2014, Narendra Modi visited Dhaka in June 2015, accompanied by Mamata Banerjee, and told Bangladeshi Prime Minister Sheikh Hasina that he was confident that cooperation between central and national governments would enable them to reach a “fair solution” on teesta. The river is woven — a network of small canals and islands — because of the huge amounts of sediment that are transported each year from the Himalayas down and accumulate on the riverbed. This results in frequent flooding and severe shoreline erosion during the monsoon, while the basin faces water shortages during the dry season.

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10 October 2021 Uncategorized Read more

Supplier Quality Agreement Pharmaceutical

It is important that these aspects, as well as other recommendations contained in the current guidelines, are taken into account when developing and implementing agreements with contractual entities. Robert Iser of PAREXEL Consulting answers questions about regulatory expectations regarding quality agreements and how companies can guarantee the quality and safety of their products. According to the FDA, a quality agreement is a comprehensive written agreement between the parties involved in the manufacture of the contract, which defines and defines the manufacturing activities of each of the parties with respect to CGMP compliance. The agreement should clearly indicate whether the owner or the contracting entity (or both) performs certain CGMP activities. 1. If a separate control laboratory is involved, all relevant roles and responsibilities should be defined. The quality agreement should explicitly specify what data is shared and how it is disseminated. An effective quality agreement defines the specific sites on which the contracting establishment will carry out manufacturing operations, including specific services to be provided at each site. Whenever a contractor or cMO is engaged, including agreements between different departments of the same undertaking, regardless of the physical location of the parties involved, a quality agreement should be concluded. The agreement should cover all aspects of the project affecting the identity, quality, safety, efficacy and purity of a product. Elements that may affect the conformity status of the contractor or customer must also be included.

A quality agreement is a comprehensive document that defines both specific quality parameters for a project and the party responsible for executing those parameters. The level of detail of a quality agreement varies depending on the development phase of the project. Iser: There are a number of important aspects of quality agreements between a pharmaceutical company and an order manufacturer. It is essential that the following aspects are clearly formulated and agreed: Robert Iser, Vice President of PAREXEL Consulting, discussed with Pharmaceutical Technology Europe the role of quality agreements in outsourcing. The FDA guidelines state (as part of case examples): “No matter who tests the products, the owners` quality units are ultimately responsible for manufacturing the products in compliance with CGMP. A quality agreement will not change that. FDA could cite the owners. because they do not evaluate, qualify, control and monitor their contractual establishments. A quality agreement should contain at least the following sections: The FDA`s current position on quality agreements is contained in the “Contract Manufacturing Arrangements for Drugs: Quality Agreements” guidelines published in 2016.

The guidelines explicitly state that manufacturing activities are the most important element of a quality agreement. It highlights the seven most critical areas that should be the subject of a quality agreement and their specific implications in terms of quality and change control. Do you have quality agreements with your payroll manufacturers, co-workers, payroll labs and component suppliers? If not, we can help you develop and implement quality agreements with your suppliers throughout your supply chain. For information on how Weinberg Group can help your company meet cGMP compliance in the pharmaceutical supply chain, contact us today. PTE: What are the FDA`s expectations for quality agreements? A true example of compliance [FDA] 483 under quality agreements is a contractual control body that is cited for failing to comply with a quality agreement on the destruction of residual samples with the authorization of the contracted company. . . .

10 October 2021 Uncategorized Read more


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