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There Is A Lot In Store For Big Pharma

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Advanced Color Measurement Strengthening Pharma QC

Achieving absolute precision in pharmaceutical manufacturing necessitates a comprehensive and rigorous oversight of physical attributes, with color serving as a primary indicator of chemical stability and composition. By integrating sophisticated instrumentation into the laboratory environment, manufacturers can transition from subjective visual assessments to standardized, data-driven methodologies that satisfy the most stringent global regulatory requirements. This strategic focus on color measurement pharma QC facilitates the early identification of raw material impurities and ensures uncompromising batch-to-batch consistency in final dosage forms, thereby bolstering patient safety and brand reputation.

GMP Compliance in Analytical Testing and Color Control

Adhering to Good Manufacturing Practices is a non-negotiable requirement for pharmaceutical organizations dedicated to maintaining global safety and quality standards. The intersection of GMP compliance color control and analytical testing ensures that every step of the production process is meticulously documented, validated, and repeatable. By focusing on the rigorous monitoring of physical attributes and chemical purity, manufacturers can mitigate the risks of contamination and stability failures, delivering high-quality healthcare products that patients and healthcare providers can trust implicitly. This disciplined approach ensures that all quality decisions are based on objective, verifiable data.

Choosing Analytical Instruments for Pharma QC Labs

Selecting the right laboratory equipment is a critical decision that directly impacts the efficiency, accuracy, and compliance of pharmaceutical operations. Evaluating analytical instruments pharma QC requirements involves a deep dive into technical specifications, vendor reliability, and the potential for long-term scalability. By choosing tools that integrate seamlessly with existing digital workflows and international regulatory standards, laboratory managers can ensure that their facility is equipped to handle the rigorous demands of modern drug testing and quality assurance. This strategic approach minimizes operational risk and ensures the delivery of safe and effective medications to patients globally.
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The Big Pharma is expecting higher gains in 2021, and surprisingly, this is not because of COVID-19. Focus on the anti-inflammatory and diabetes drugs has kept the spirits high with new clinical data being given a lot of thrust. Lilly and Abbvie have shown an inclination towards their flagship drugs so much so that it has resulted in a positive impact on their stock prices too.

The worldโ€™s largest publicly traded pharmaceutical companies are expecting a healthy 2021. And by the way, this has nothing to do with the current coronavirus pandemic. Eli Lilly in a statement has said that it is expecting a profit of $26.5 billion to $28 billion next year, which is almost about 11% higher than this yearโ€™s forecast. This growth can be attributed to drugs such as Trulicity & Taltz that are already on the market. The company has boosted its dividend payout by 15% and the shares also seem to be rising. Lilly has already made it crystal clear on its expansion plans as well with a deal to acquire gene therapy startup Prevail Therapeutics for $880 million in upfront cash.

Similarly, Abbvie has increased its long term guidance to immunology drugs, Rinvoq & Skyrizi. The company is expecting a revenue of $15 billion by 2025 which is higher from the previous forecast of $10 billion. Although this looks a pretty steep target going by the numbers in the first 09 months of 2020 where they were pegged at $1.3 billion, the recent clinical data shows Rinvoq to be more effective for atopic dermatitis patients. The pandemic has slowed down the development of various other drugs, but dermatology remains an exception as it is a very lucrative and enhanced market.

It is a known fact that Abbvie today faces a cheap competitor in Humira in the US, especially in the anti-inflammatory segment. Humira is almost $15 billion in global sales making it the worldโ€™s best-selling drug and also accounts for more than half of the companyโ€™s total sales. All this speaks very highly about the vision of these companies as they arenโ€™t banking on the COVID-19 treatments. The fact is that the duration of the pandemic, as well as sales opportunities coming from it, remain uncertain for the Pharmaceutical companies. Now that the COVID 19 vaccines have started getting distributed, Wall Street in all likelihood shall place a low value on the profits from drugs like Lillyโ€™s COVID-19 antibody treatment. The company is expecting somewhere around $1 billion to $2 billion from the sales related to COVID-19ย  next year. It further plans to spend around $300 to $400 million on the research related to the pandemic. However, come to think of it, the impact of the pandemic on Abbvieโ€™s overall performance is going to be minimal.

Lilly is trading at 21 times this yearโ€™s adjusted profit forecast, whereas Abbvie is trading at 10. Both their businesses are highly undistributed by the course of the pandemic and hence make them a huge attraction amongst investors. The industry has also become more cozy with risks such as tougher regulations that are laid on prescription drug prices.

World Pharma Today brings together the global pharmaceutical industry โ€” from R&D leaders and regulatory affairs professionals to manufacturers and distribution executives โ€” through trusted editorial, market intelligence, and digital engagement.

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Related stories

Advanced Color Measurement Strengthening Pharma QC

Achieving absolute precision in pharmaceutical manufacturing necessitates a comprehensive and rigorous oversight of physical attributes, with color serving as a primary indicator of chemical stability and composition. By integrating sophisticated instrumentation into the laboratory environment, manufacturers can transition from subjective visual assessments to standardized, data-driven methodologies that satisfy the most stringent global regulatory requirements. This strategic focus on color measurement pharma QC facilitates the early identification of raw material impurities and ensures uncompromising batch-to-batch consistency in final dosage forms, thereby bolstering patient safety and brand reputation.

GMP Compliance in Analytical Testing and Color Control

Adhering to Good Manufacturing Practices is a non-negotiable requirement for pharmaceutical organizations dedicated to maintaining global safety and quality standards. The intersection of GMP compliance color control and analytical testing ensures that every step of the production process is meticulously documented, validated, and repeatable. By focusing on the rigorous monitoring of physical attributes and chemical purity, manufacturers can mitigate the risks of contamination and stability failures, delivering high-quality healthcare products that patients and healthcare providers can trust implicitly. This disciplined approach ensures that all quality decisions are based on objective, verifiable data.

Choosing Analytical Instruments for Pharma QC Labs

Selecting the right laboratory equipment is a critical decision that directly impacts the efficiency, accuracy, and compliance of pharmaceutical operations. Evaluating analytical instruments pharma QC requirements involves a deep dive into technical specifications, vendor reliability, and the potential for long-term scalability. By choosing tools that integrate seamlessly with existing digital workflows and international regulatory standards, laboratory managers can ensure that their facility is equipped to handle the rigorous demands of modern drug testing and quality assurance. This strategic approach minimizes operational risk and ensures the delivery of safe and effective medications to patients globally.

Spectrophotometers Driving Accuracy in Drug Quality

Precision in pharmaceutical analysis is fundamental to ensuring that every therapeutic agent delivered to a patient meets the highest safety and efficacy standards. The implementation of high-grade spectrophotometers drug quality control workflows provides a scientific basis for quantifying chemical properties and physical characteristics with unmatched reliability. By leveraging advanced spectral data, manufacturers can validate formulations and detect impurities early in the production cycle, thereby reinforcing the integrity of the global supply chain, ensuring regulatory compliance, and protecting the well-being of patients around the world.

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Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

โ€“ Access theMedia Pack Now

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