�ݺ�ߣshows by User: MohiniTawade

�ݺ�ߣshows by User: MohiniTawade / http://www.slideshare.net/images/logo.gif �ݺ�ߣshows by User: MohiniTawade / Sat, 20 Jan 2024 18:11:46 GMT �ݺ�ߣShare feed for �ݺ�ߣshows by User: MohiniTawade Pharmaceutical validation /slideshow/pharmaceutical-validation-730a/265597087 pharmaceuticalvalidationftir1-240120181146-fcda7803
QUALIFICATION OF ANALYTICAL EQUIPMENT]]>
QUALIFICATION OF ANALYTICAL EQUIPMENT]]> Sat, 20 Jan 2024 18:11:46 GMT /slideshow/pharmaceutical-validation-730a/265597087 MohiniTawade@slideshare.net(MohiniTawade) Pharmaceutical validation MohiniTawade QUALIFICATION OF ANALYTICAL EQUIPMENT <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/pharmaceuticalvalidationftir1-240120181146-fcda7803-thumbnail.jpg?width=120&height=120&fit=bounds" /> QUALIFICATION OF ANALYTICAL EQUIPMENT

Pharmaceutical validation from MohiniTawade

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0 Hazard And Risk Management.pdf /slideshow/hazard-and-risk-managementpdf/265596844 hazardandriskmanagement-240120175448-af97c1df
Situation that posses a level of threat to life, health, property, or environment. Hazard Management involves identifying hazard, assessing the hazard, and controlling the risk.]]>
Situation that posses a level of threat to life, health, property, or environment. Hazard Management involves identifying hazard, assessing the hazard, and controlling the risk.]]> Sat, 20 Jan 2024 17:54:48 GMT /slideshow/hazard-and-risk-managementpdf/265596844 MohiniTawade@slideshare.net(MohiniTawade) Hazard And Risk Management.pdf MohiniTawade Situation that posses a level of threat to life, health, property, or environment. Hazard Management involves identifying hazard, assessing the hazard, and controlling the risk. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/hazardandriskmanagement-240120175448-af97c1df-thumbnail.jpg?width=120&height=120&fit=bounds" /> Situation that posses a level of threat to life, health, property, or environment. Hazard Management involves identifying hazard, assessing the hazard, and controlling the risk.

Hazard And Risk Management.pdf from MohiniTawade

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0 Advaced sterile product manufacturing technology.pdf /slideshow/advaced-sterile-product-manufacturing-technologypdf/260668750 advacedsterileproductmanufacturingtechnology-230907170913-e1c0cc9f
Advanced manufacturing is the use of innovative technology to improve products or processes It can be defined as “The rate of technology adaptation and the ability to use that technology to remain competitive and add value to the advanced manufacturing sectors” In advanced aseptic processes, direct contact of the open product with an operator wearing a conventional cleanroom garment is not allowed Isolators effectively provide a seal against the entry of external contaminants using air over-pressure. ]]>
Advanced manufacturing is the use of innovative technology to improve products or processes It can be defined as “The rate of technology adaptation and the ability to use that technology to remain competitive and add value to the advanced manufacturing sectors” In advanced aseptic processes, direct contact of the open product with an operator wearing a conventional cleanroom garment is not allowed Isolators effectively provide a seal against the entry of external contaminants using air over-pressure. ]]> Thu, 07 Sep 2023 17:09:13 GMT /slideshow/advaced-sterile-product-manufacturing-technologypdf/260668750 MohiniTawade@slideshare.net(MohiniTawade) Advaced sterile product manufacturing technology.pdf MohiniTawade Advanced manufacturing is the use of innovative technology to improve products or processes It can be defined as “The rate of technology adaptation and the ability to use that technology to remain competitive and add value to the advanced manufacturing sectors” In advanced aseptic processes, direct contact of the open product with an operator wearing a conventional cleanroom garment is not allowed Isolators effectively provide a seal against the entry of external contaminants using air over-pressure. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/advacedsterileproductmanufacturingtechnology-230907170913-e1c0cc9f-thumbnail.jpg?width=120&height=120&fit=bounds" /> Advanced manufacturing is the use of innovative technology to improve products or processes It can be defined as “The rate of technology adaptation and the ability to use that technology to remain competitive and add value to the advanced manufacturing sectors” In advanced aseptic processes, direct contact of the open product with an operator wearing a conventional cleanroom garment is not allowed Isolators effectively provide a seal against the entry of external contaminants using air over-pressure.

Advaced sterile product manufacturing technology.pdf from MohiniTawade

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0 Models of Technology Transfer.pdf /slideshow/models-of-technology-transferpdf/257706892 modelsoftechnologytransfer-230506092931-c9b26205
Transferring of details related to formulation and analytical strategies from one area to another area i.e. from R&D to production department and transferring of resulting product from lab scale to production scale. It’s a organized procedure including documented information and knowledge gained throughout the development. In pharmaceutical industry technology transfer includes steps from drug discovery to product development, clinical trials and full scale commercialization. According to WHO it’s a logical procedure that controls the transfer of any method along with its documentation and professional expertise between development and manufacturer. ]]>
Transferring of details related to formulation and analytical strategies from one area to another area i.e. from R&D to production department and transferring of resulting product from lab scale to production scale. It’s a organized procedure including documented information and knowledge gained throughout the development. In pharmaceutical industry technology transfer includes steps from drug discovery to product development, clinical trials and full scale commercialization. According to WHO it’s a logical procedure that controls the transfer of any method along with its documentation and professional expertise between development and manufacturer. ]]> Sat, 06 May 2023 09:29:31 GMT /slideshow/models-of-technology-transferpdf/257706892 MohiniTawade@slideshare.net(MohiniTawade) Models of Technology Transfer.pdf MohiniTawade Transferring of details related to formulation and analytical strategies from one area to another area i.e. from R&D to production department and transferring of resulting product from lab scale to production scale. It’s a organized procedure including documented information and knowledge gained throughout the development. In pharmaceutical industry technology transfer includes steps from drug discovery to product development, clinical trials and full scale commercialization. According to WHO it’s a logical procedure that controls the transfer of any method along with its documentation and professional expertise between development and manufacturer. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/modelsoftechnologytransfer-230506092931-c9b26205-thumbnail.jpg?width=120&height=120&fit=bounds" /> Transferring of details related to formulation and analytical strategies from one area to another area i.e. from R&D to production department and transferring of resulting product from lab scale to production scale. It’s a organized procedure including documented information and knowledge gained throughout the development. In pharmaceutical industry technology transfer includes steps from drug discovery to product development, clinical trials and full scale commercialization. According to WHO it’s a logical procedure that controls the transfer of any method along with its documentation and professional expertise between development and manufacturer.

Models of Technology Transfer.pdf from MohiniTawade

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0 HACCP.pdf /slideshow/haccppdf-257536124/257536124 haccp-230424081554-4ee7bee5
Hazard Analysis And Critical Control Point (HAPPC). HAPPC is systemic approach for identification, evaluation and control of food safety hazards. Preventing the problems from occurring is the primary goal of HACCP system. It is logical, scientific approach which controls safety problems in food products. Safety control needs to be monitored in production system related to biological, chemical and physical hazard. ]]>
Hazard Analysis And Critical Control Point (HAPPC). HAPPC is systemic approach for identification, evaluation and control of food safety hazards. Preventing the problems from occurring is the primary goal of HACCP system. It is logical, scientific approach which controls safety problems in food products. Safety control needs to be monitored in production system related to biological, chemical and physical hazard. ]]> Mon, 24 Apr 2023 08:15:54 GMT /slideshow/haccppdf-257536124/257536124 MohiniTawade@slideshare.net(MohiniTawade) HACCP.pdf MohiniTawade Hazard Analysis And Critical Control Point (HAPPC). HAPPC is systemic approach for identification, evaluation and control of food safety hazards. Preventing the problems from occurring is the primary goal of HACCP system. It is logical, scientific approach which controls safety problems in food products. Safety control needs to be monitored in production system related to biological, chemical and physical hazard. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/haccp-230424081554-4ee7bee5-thumbnail.jpg?width=120&height=120&fit=bounds" /> Hazard Analysis And Critical Control Point (HAPPC). HAPPC is systemic approach for identification, evaluation and control of food safety hazards. Preventing the problems from occurring is the primary goal of HACCP system. It is logical, scientific approach which controls safety problems in food products. Safety control needs to be monitored in production system related to biological, chemical and physical hazard.

HACCP.pdf from MohiniTawade

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0 Design and Construction of plant as per the GMP Guidelines.pdf /slideshow/design-and-construction-of-plant-as-per-gmp-guidelinespdf/256819078 designandconstructionofplantaspergmpguidelines-230324174645-9ee4c840
GMP is that part of Quality assurance which ensures that the products are consistently manufactured and controlled to the Quality standards appropriate to their intended use ]]>
GMP is that part of Quality assurance which ensures that the products are consistently manufactured and controlled to the Quality standards appropriate to their intended use ]]> Fri, 24 Mar 2023 17:46:45 GMT /slideshow/design-and-construction-of-plant-as-per-gmp-guidelinespdf/256819078 MohiniTawade@slideshare.net(MohiniTawade) Design and Construction of plant as per the GMP Guidelines.pdf MohiniTawade GMP is that part of Quality assurance which ensures that the products are consistently manufactured and controlled to the Quality standards appropriate to their intended use <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/designandconstructionofplantaspergmpguidelines-230324174645-9ee4c840-thumbnail.jpg?width=120&height=120&fit=bounds" /> GMP is that part of Quality assurance which ensures that the products are consistently manufactured and controlled to the Quality standards appropriate to their intended use

Design and Construction of plant as per the GMP Guidelines.pdf from MohiniTawade

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0 Affinity Chromatography.pdf /slideshow/affinity-chromatographypdf-256604667/256604667 affinitychromatography-230318055826-17997e27
Affinity Chromatography involves the covalent attachment of an immobilized biochemical called as affinity ligand to a solid support. When a sample is passed through the column, only solute that selectively binds to the complementary ligand is retained; other sample components elute without retention. The separation exploit the “lock and key” binding that is prevalent in biological systems. The retention solutes can be eluted from the column by changing the mobile phase composition. ]]>
Affinity Chromatography involves the covalent attachment of an immobilized biochemical called as affinity ligand to a solid support. When a sample is passed through the column, only solute that selectively binds to the complementary ligand is retained; other sample components elute without retention. The separation exploit the “lock and key” binding that is prevalent in biological systems. The retention solutes can be eluted from the column by changing the mobile phase composition. ]]> Sat, 18 Mar 2023 05:58:26 GMT /slideshow/affinity-chromatographypdf-256604667/256604667 MohiniTawade@slideshare.net(MohiniTawade) Affinity Chromatography.pdf MohiniTawade Affinity Chromatography involves the covalent attachment of an immobilized biochemical called as affinity ligand to a solid support. When a sample is passed through the column, only solute that selectively binds to the complementary ligand is retained; other sample components elute without retention. The separation exploit the “lock and key” binding that is prevalent in biological systems. The retention solutes can be eluted from the column by changing the mobile phase composition. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/affinitychromatography-230318055826-17997e27-thumbnail.jpg?width=120&height=120&fit=bounds" /> Affinity Chromatography involves the covalent attachment of an immobilized biochemical called as affinity ligand to a solid support. When a sample is passed through the column, only solute that selectively binds to the complementary ligand is retained; other sample components elute without retention. The separation exploit the “lock and key” binding that is prevalent in biological systems. The retention solutes can be eluted from the column by changing the mobile phase composition.

Affinity Chromatography.pdf from MohiniTawade

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0 Master formula record.pdf /slideshow/master-formula-recordpdf/256141611 masterformularecord-230227085415-3d2272a9
Master Formula Record (MFR) is a master document for any pharmaceutical product. MFR contains all information about the manufacturing process for the product. MFR is prepared by the research and development team of the company. MFR is used as reference standard for preparing batch manufacturing record (BMR) by manufacturing units. ]]>
Master Formula Record (MFR) is a master document for any pharmaceutical product. MFR contains all information about the manufacturing process for the product. MFR is prepared by the research and development team of the company. MFR is used as reference standard for preparing batch manufacturing record (BMR) by manufacturing units. ]]> Mon, 27 Feb 2023 08:54:14 GMT /slideshow/master-formula-recordpdf/256141611 MohiniTawade@slideshare.net(MohiniTawade) Master formula record.pdf MohiniTawade Master Formula Record (MFR) is a master document for any pharmaceutical product. MFR contains all information about the manufacturing process for the product. MFR is prepared by the research and development team of the company. MFR is used as reference standard for preparing batch manufacturing record (BMR) by manufacturing units. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/masterformularecord-230227085415-3d2272a9-thumbnail.jpg?width=120&height=120&fit=bounds" /> Master Formula Record (MFR) is a master document for any pharmaceutical product. MFR contains all information about the manufacturing process for the product. MFR is prepared by the research and development team of the company. MFR is used as reference standard for preparing batch manufacturing record (BMR) by manufacturing units.

Master formula record.pdf from MohiniTawade

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0 McKinsey 7s model.pdf /slideshow/mckinsey-7s-modelpdf/255785746 mckinsey7smodel-230209165351-be9f45da
The McKinsey 7-S model is a useful tool that can be used to diagnose and solve organizational problems. It depicts an organization as a collection of seven interconnected elements: structure, strategy, systems, staff, skills, style and shared values. By considering how each of these elements impacts on the others, it is possible to take a holistic approach to organizational change. ]]>
The McKinsey 7-S model is a useful tool that can be used to diagnose and solve organizational problems. It depicts an organization as a collection of seven interconnected elements: structure, strategy, systems, staff, skills, style and shared values. By considering how each of these elements impacts on the others, it is possible to take a holistic approach to organizational change. ]]> Thu, 09 Feb 2023 16:53:51 GMT /slideshow/mckinsey-7s-modelpdf/255785746 MohiniTawade@slideshare.net(MohiniTawade) McKinsey 7s model.pdf MohiniTawade The McKinsey 7-S model is a useful tool that can be used to diagnose and solve organizational problems. It depicts an organization as a collection of seven interconnected elements: structure, strategy, systems, staff, skills, style and shared values. By considering how each of these elements impacts on the others, it is possible to take a holistic approach to organizational change. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/mckinsey7smodel-230209165351-be9f45da-thumbnail.jpg?width=120&height=120&fit=bounds" /> The McKinsey 7-S model is a useful tool that can be used to diagnose and solve organizational problems. It depicts an organization as a collection of seven interconnected elements: structure, strategy, systems, staff, skills, style and shared values. By considering how each of these elements impacts on the others, it is possible to take a holistic approach to organizational change.

McKinsey 7s model.pdf from MohiniTawade

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0 Black Pepper /MohiniTawade/black-pepper-252035589 blackpepper-220622060736-01899ec3
Black pepper, phytoconstituents and it's marketed preparations]]>
Black pepper, phytoconstituents and it's marketed preparations]]> Wed, 22 Jun 2022 06:07:36 GMT /MohiniTawade/black-pepper-252035589 MohiniTawade@slideshare.net(MohiniTawade) Black Pepper MohiniTawade Black pepper, phytoconstituents and it's marketed preparations <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/blackpepper-220622060736-01899ec3-thumbnail.jpg?width=120&height=120&fit=bounds" /> Black pepper, phytoconstituents and it's marketed preparations

Black Pepper from MohiniTawade

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0 Processing and preparations for market :Turmeric /slideshow/processing-and-preparations-for-market-turmeric/246716581 seminar51to57-210422053751
Processing and preparations for market : Turmeric]]>
Processing and preparations for market : Turmeric]]> Thu, 22 Apr 2021 05:37:50 GMT /slideshow/processing-and-preparations-for-market-turmeric/246716581 MohiniTawade@slideshare.net(MohiniTawade) Processing and preparations for market :Turmeric MohiniTawade Processing and preparations for market : Turmeric <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/seminar51to57-210422053751-thumbnail.jpg?width=120&height=120&fit=bounds" /> Processing and preparations for market : Turmeric

Processing and preparations for market :Turmeric from MohiniTawade

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0 https://cdn.slidesharecdn.com/profile-photo-MohiniTawade-48x48.jpg?cb=1721850059 www.researchgate.net/profile/Mohini-Tawade https://cdn.slidesharecdn.com/ss_thumbnails/pharmaceuticalvalidationftir1-240120181146-fcda7803-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/pharmaceutical-validation-730a/265597087 Pharmaceutical validation https://cdn.slidesharecdn.com/ss_thumbnails/hazardandriskmanagement-240120175448-af97c1df-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/hazard-and-risk-managementpdf/265596844 Hazard And Risk Manage... https://cdn.slidesharecdn.com/ss_thumbnails/advacedsterileproductmanufacturingtechnology-230907170913-e1c0cc9f-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/advaced-sterile-product-manufacturing-technologypdf/260668750 Advaced sterile produc...