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  • We assist start-ups in faster emergence and established companies in digitalizing smoothly. The development office is located in Eastern Europe and Asia with the headquarters in the Netherlands (Amsterdam) and the USA (Las Vegas). Attract Group has been successfully operating on the market since 2011 and has proven its expertise. Our team consists of highly skilled specialists in all branches namely web development, web design, project architecture, application development, and IT Business Consulting.
    We assist start-ups in faster emergence and established companies in digitalizing smoothly. The development office is located in Eastern Europe and Asia with the headquarters in the Netherlands (Amsterdam) and the USA (Las Vegas). Attract Group has been successfully operating on the market since 2011 and has proven its expertise. Our team consists of highly skilled specialists in all branches namely web development, web design, project architecture, application development, and IT Business Consulting.
    ATTRACTGROUP.COM
    Retail Loyalty Program Strategies That Will Be Effective in 2024
    Stay ahead in retail with loyalty program strategies for 2024. Learn how to build customer loyalty and increase retention. Read our expert tips now!
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  • https://www.mrobusinesstoday.com/ametek-mro-consolidates-european-business-jet-component-capabilities/
    https://www.mrobusinesstoday.com/ametek-mro-consolidates-european-business-jet-component-capabilities/
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  • Flat rates follow a strong run on big lanes out of China – driven mainly by e-commerce activity.

    #TACIndex #Baltic AirFreightIndex #China #HongKong #Europe #US #aircargo #aircraft #ecommerce
    Flat rates follow a strong run on big lanes out of China – driven mainly by e-commerce activity. #TACIndex #Baltic AirFreightIndex #China #HongKong #Europe #US #aircargo #aircraft #ecommerce
    WWW.STATTIMES.COM
    Global air freight rates unchanged ahead of low season: TAC Index
    Flat rates follow a strong run on big lanes out of China – driven mainly by e-commerce activity.
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  • First European cargo airline to connect Europe with Monterrey; new belly destinations from Munich

    #LufthansaCargo #Lufthansa #Monterrey #Mexico #Frankfurt #Munich #Europe
    First European cargo airline to connect Europe with Monterrey; new belly destinations from Munich #LufthansaCargo #Lufthansa #Monterrey #Mexico #Frankfurt #Munich #Europe
    WWW.STATTIMES.COM
    Lufthansa Cargo adds Monterrey to freighter flight schedule
    First European cargo airline to connect Europe with Monterrey; new belly destinations from Munich
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  • The new gateway, modelled after operations in Atlanta, Chicago, and Los Angeles, will focus on transhipping European and Asian cargo via Miami to Latin America.

    #APMollerMaersk #Maersk #Atlanta #Chicago #LosAngeles #Miami #LatinAmerica #aircargo #aircraft
    The new gateway, modelled after operations in Atlanta, Chicago, and Los Angeles, will focus on transhipping European and Asian cargo via Miami to Latin America. #APMollerMaersk #Maersk #Atlanta #Chicago #LosAngeles #Miami #LatinAmerica #aircargo #aircraft
    WWW.STATTIMES.COM
    Maersk launches air freight gateway in Miami
    The new gateway, modelled after operations in Atlanta, Chicago, and Los Angeles, will focus on transhipping European and Asian cargo via Miami to Latin America.
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  • After several months in development, MSC Mediterranean Shipping Company announced the launch of MSC Air Cargo in September 2022 as a complementary service to its container shipping solutions. Two months later, in December, the Geneva-headquartered all-cargo carrier launched its first commercial operations from its European gateway at Liege in Belgium. With a fleet of four brand new Boeing 777 freighters, and a fifth one expected to join the fleet soon, the 20-month-old cargo-carrier has impressed the air cargo market with innovative solutions to fulfill market demands leveraging technology and customer-first approach. Its charter solution is expansive and has a dedicated team to fulfil unique demands.

    #MSCAirCargo #MSCCargo #MSCMediterraneanShippingCompany #Boeing #Boeing777freighters #aircargo #aircraft
    After several months in development, MSC Mediterranean Shipping Company announced the launch of MSC Air Cargo in September 2022 as a complementary service to its container shipping solutions. Two months later, in December, the Geneva-headquartered all-cargo carrier launched its first commercial operations from its European gateway at Liege in Belgium. With a fleet of four brand new Boeing 777 freighters, and a fifth one expected to join the fleet soon, the 20-month-old cargo-carrier has impressed the air cargo market with innovative solutions to fulfill market demands leveraging technology and customer-first approach. Its charter solution is expansive and has a dedicated team to fulfil unique demands. #MSCAirCargo #MSCCargo #MSCMediterraneanShippingCompany #Boeing #Boeing777freighters #aircargo #aircraft
    WWW.STATTIMES.COM
    Cargo charters: Tailor-made and innovative
    After several months in development, MSC Mediterranean Shipping Company announced the launch of MSC Air Cargo in September 2022 as a complementary service to its container shipping solutions. Two...
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  • Hardness test block malaysia

    Yamamoto Hardness Test Blocks Supply Malaysia - Takumi

    Takumi Precision supplies the Yamamoto Hardness Test Blocks in Malaysia. YSTL's hardness blocks are used in many countries throughout Europe, America, etc.

    https://takumiprecision.com.my/product/hardness-test-block/yamamoto-hardness-test-blocks/
    Hardness test block malaysia Yamamoto Hardness Test Blocks Supply Malaysia - Takumi Takumi Precision supplies the Yamamoto Hardness Test Blocks in Malaysia. YSTL's hardness blocks are used in many countries throughout Europe, America, etc. https://takumiprecision.com.my/product/hardness-test-block/yamamoto-hardness-test-blocks/
    TAKUMIPRECISION.COM.MY
    Yamamoto Hardness Test Blocks Supply Malaysia - Takumi
    Takumi Precision supplies the Yamamoto Hardness Test Blocks in Malaysia. YSTL’s hardness blocks are used in many countries throughout Europe, America, etc.
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  • Bilberry Supplements

    What Is Bilberry?
    The bilberry is a small, dark blue or purple berry that grows on the Vaccinium myrtillus shrub. It is native to Europe but can also be found in some parts of North America. It is closely related to other berries like blueberries, cranberries, and huckleberries.

    https://www.nationalnutrition.ca/eye/bilberry.html

    #bilberry
    Bilberry Supplements What Is Bilberry? The bilberry is a small, dark blue or purple berry that grows on the Vaccinium myrtillus shrub. It is native to Europe but can also be found in some parts of North America. It is closely related to other berries like blueberries, cranberries, and huckleberries. https://www.nationalnutrition.ca/eye/bilberry.html #bilberry
    WWW.NATIONALNUTRITION.CA
    Buy Bilberry Supplements | Eye Health Supplements & Vitamins at NationalNutrition.ca
    Shop Bilberry Eye Health Supplements & Vitamins | Discover the benefits of Bilberry for improving vision and reducing eye fatigue. Available now at NationalNutrition.ca.
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  • Regulatory Compliance Considerations in Topical Clinical Manufacturing CDMO Services

    Regulatory compliance is of paramount importance in topical clinical manufacturing Contract Development and Manufacturing Organization (CDMO) services to ensure adherence to applicable regulations, standards, and guidelines governing the development, manufacturing, and distribution of topical pharmaceutical products. Commercial manufacturing CDMOs must navigate a complex regulatory landscape to meet regulatory requirements, obtain necessary approvals, and maintain compliance throughout the product lifecycle. Let's explore the regulatory compliance considerations in topical clinical manufacturing CDMO services:

    Good Manufacturing Practice (GMP) Compliance: Commercial manufacturing CDMOs must adhere to Good Manufacturing Practice (GMP) regulations established by regulatory authorities such as the U.S. Food and Drug Administration (FDA), European Medicines Agency (EMA), and other regulatory agencies worldwide. GMP guidelines outline requirements for the design, operation, and control of manufacturing facilities, equipment, processes, and personnel to ensure the quality, safety, and efficacy of pharmaceutical products, including topical formulations.
    ICH Guidelines: The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) develops guidelines and harmonized standards for pharmaceutical development, including topical drug products. Commercial manufacturing CDMOs must comply with ICH guidelines such as ICH Q8 (Pharmaceutical Development), ICH Q9 (Quality Risk Management), and ICH Q10 (Pharmaceutical Quality System) to ensure a systematic approach to pharmaceutical development, risk management, and quality assurance.
    Drug Master File (DMF) Submission: Commercial manufacturing CDMOs may be required to prepare and submit Drug Master Files (DMFs) to regulatory authorities as part of the regulatory approval process for topical pharmaceutical products. DMFs contain detailed information on the manufacturing processes, quality control procedures, and specifications of raw materials, intermediates, and finished products, providing regulatory agencies with essential information to evaluate product quality and safety.
    Product Registration and Marketing Authorization: Commercial manufacturing CDMOs collaborate with pharmaceutical sponsors and regulatory authorities to obtain product registration and marketing authorization for topical pharmaceutical products. This process involves submitting regulatory filings, dossiers, and registration documents, conducting preclinical and clinical studies, and demonstrating product safety, efficacy, and quality to regulatory agencies for approval.
    Labeling and Packaging Compliance: Commercial manufacturing CDMOs must ensure that labeling and packaging of topical pharmaceutical products comply with regulatory requirements and guidelines. Labeling requirements include accurate and comprehensive product information, including active ingredients, dosage form, strength, dosage instructions, warnings, precautions, and storage conditions, as well as compliance with applicable labeling regulations such as FDA regulations for over-the-counter (OTC) drug products.
    Post-Marketing Surveillance: Commercial manufacturing CDMOs participate in post-marketing surveillance activities to monitor the safety, efficacy, and quality of topical pharmaceutical products following regulatory approval and commercialization. Post-marketing surveillance involves collecting and analyzing adverse event reports, conducting pharmacovigilance activities, and implementing corrective actions or product recalls as necessary to ensure patient safety and regulatory compliance.
    By prioritizing regulatory compliance considerations in topical clinical manufacturing CDMO services, commercial manufacturing CDMOs demonstrate their commitment to quality, safety, and compliance with regulatory requirements, ensuring the timely approval, commercialization, and availability of high-quality topical pharmaceutical products for patients worldwide. For more information on regulatory compliance considerations in topical clinical manufacturing CDMO services, please visit https://renejix.com/pharmaceutical-manufacturing/commercial-manufacturing/
    Regulatory Compliance Considerations in Topical Clinical Manufacturing CDMO Services Regulatory compliance is of paramount importance in topical clinical manufacturing Contract Development and Manufacturing Organization (CDMO) services to ensure adherence to applicable regulations, standards, and guidelines governing the development, manufacturing, and distribution of topical pharmaceutical products. Commercial manufacturing CDMOs must navigate a complex regulatory landscape to meet regulatory requirements, obtain necessary approvals, and maintain compliance throughout the product lifecycle. Let's explore the regulatory compliance considerations in topical clinical manufacturing CDMO services: Good Manufacturing Practice (GMP) Compliance: Commercial manufacturing CDMOs must adhere to Good Manufacturing Practice (GMP) regulations established by regulatory authorities such as the U.S. Food and Drug Administration (FDA), European Medicines Agency (EMA), and other regulatory agencies worldwide. GMP guidelines outline requirements for the design, operation, and control of manufacturing facilities, equipment, processes, and personnel to ensure the quality, safety, and efficacy of pharmaceutical products, including topical formulations. ICH Guidelines: The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) develops guidelines and harmonized standards for pharmaceutical development, including topical drug products. Commercial manufacturing CDMOs must comply with ICH guidelines such as ICH Q8 (Pharmaceutical Development), ICH Q9 (Quality Risk Management), and ICH Q10 (Pharmaceutical Quality System) to ensure a systematic approach to pharmaceutical development, risk management, and quality assurance. Drug Master File (DMF) Submission: Commercial manufacturing CDMOs may be required to prepare and submit Drug Master Files (DMFs) to regulatory authorities as part of the regulatory approval process for topical pharmaceutical products. DMFs contain detailed information on the manufacturing processes, quality control procedures, and specifications of raw materials, intermediates, and finished products, providing regulatory agencies with essential information to evaluate product quality and safety. Product Registration and Marketing Authorization: Commercial manufacturing CDMOs collaborate with pharmaceutical sponsors and regulatory authorities to obtain product registration and marketing authorization for topical pharmaceutical products. This process involves submitting regulatory filings, dossiers, and registration documents, conducting preclinical and clinical studies, and demonstrating product safety, efficacy, and quality to regulatory agencies for approval. Labeling and Packaging Compliance: Commercial manufacturing CDMOs must ensure that labeling and packaging of topical pharmaceutical products comply with regulatory requirements and guidelines. Labeling requirements include accurate and comprehensive product information, including active ingredients, dosage form, strength, dosage instructions, warnings, precautions, and storage conditions, as well as compliance with applicable labeling regulations such as FDA regulations for over-the-counter (OTC) drug products. Post-Marketing Surveillance: Commercial manufacturing CDMOs participate in post-marketing surveillance activities to monitor the safety, efficacy, and quality of topical pharmaceutical products following regulatory approval and commercialization. Post-marketing surveillance involves collecting and analyzing adverse event reports, conducting pharmacovigilance activities, and implementing corrective actions or product recalls as necessary to ensure patient safety and regulatory compliance. By prioritizing regulatory compliance considerations in topical clinical manufacturing CDMO services, commercial manufacturing CDMOs demonstrate their commitment to quality, safety, and compliance with regulatory requirements, ensuring the timely approval, commercialization, and availability of high-quality topical pharmaceutical products for patients worldwide. For more information on regulatory compliance considerations in topical clinical manufacturing CDMO services, please visit https://renejix.com/pharmaceutical-manufacturing/commercial-manufacturing/
    RENEJIX.COM
    Commercial Manufacturing
    Elevate your commercial manufacturing with our superior CDMO services. From formulation to scale-up, trust us for seamless production success.
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  • With the acquisition of Brummer, its partner in the European Food Network for the transport of temperature-controlled food between Germany, Austria, and neighbouring countries, DACHSER is strengthening its network for the transport and storage of food in Europe.

    #DACHSER #BrummerLogistik #BrummerLogisticSolutions #BrummerGroup #Germany #Austria #logistics
    With the acquisition of Brummer, its partner in the European Food Network for the transport of temperature-controlled food between Germany, Austria, and neighbouring countries, DACHSER is strengthening its network for the transport and storage of food in Europe. #DACHSER #BrummerLogistik #BrummerLogisticSolutions #BrummerGroup #Germany #Austria #logistics
    WWW.STATTIMES.COM
    DACHSER acquires food logistics provider Brummer
    With the acquisition of Brummer, its partner in the European Food Network for the transport of temperature-controlled food between Germany, Austria, and neighbouring countries, DACHSER is...
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