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DDReg Pharma

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benfits of ISO 27001 Certification

Why is an ISO 27001 Certification Important For an Organization?

In a technology-driven era where businesses are increasingly incorporating advanced information and data management tools into their operations, the risk of facing cyber attacks and breaches is also increasing. Additionally, businesses face non-compliance in regulatory and legal requirements when handing information security, and so the demand for transparent information security is on the rise- particularly […]

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RIMS Tools in Asia Market

Role of Regulatory Information Management Systems -RIMS Tools in Asia Market

Managing regulatory information for a pharmaceutical product along all stages of its life cycle is a key challenge in the pharmaceutical industry. Now, as more opportunity markets emerge bringing their own stringent regulations and changes in previous regulations, managing regulatory information is becoming increasingly complex which can delay market access for products. Furthermore, information is

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Regulatory Affairs in Pharmaceutical

Role of Regulatory Affairs in the Pharmaceutical Industry

The pharmaceutical industry is highly regulated using legislations and regulations that bring together administrative, technical, and legal information about a medicinal product. These can be a combination of guidelines, procedures, policies, etc., that pharmaceutical organizations must adhere to, or follow, to get market approval for their products. This way, governments and their relative health authorities

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Pharmacovigilance

India’s New Drugs, Medical Devices and Cosmetics Bill 2022

Drug laws & regulations in India have roots that are almost 80 years old. India still follows drug laws that were framed in pre-independence time through Drugs & Cosmetics Act – 1940 and Rules 1945. The laws & rules have frequently been amended to address the challenges posed by Indian pharma Industry. However, the basic

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DDReg Foundation Day Celebrates

DDReg celebrates its 13th Foundation Day

On Friday 1st July 2022, DDReg Pharma wholeheartedly celebrated its 13th Foundation Day. Employees from the Gurgaon, Mumbai, and Hyderabad offices connected virtually to commemorate not only the grand occasion but also each other’s milestones and achievements. The day consisted of fun activities including interactive games and performances by employees such as singing, instruments, poetry,

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Quality Management Maturity Program

Quality Management Maturity Program by the CDER of the U.S. FDA

The pharmaceutical industry is one that is constantly growing and simultaneously facing challenges in Quality Management Maturity Program in US FDA. The onset of the pandemic has brought new obstacles that require immediate attention and innovative solutions. Quality assurance (QA) is a routine measure that ultimately ensures patient safety by making sure all pharmaceutical products

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Transformation in Pharmacovigilance

Technological Transformation in Pharmacovigilance

Technological disruption is rapidly occurring across all industries. In the pharmaceutical industry, technological contenders are gradually transforming the landscape of drug development, clinical trials, and pre-clinical phases. Indeed, this holds true for Transformation Pharmacovigilance and drug safety monitoring. Though the area of the industry is niche and highly regulated, hence the apprehension in incorporating technology

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Regulatory Compliance Outsourcing solutions provider in pharmaceutical industry

Regulatory Compliance Outsourcing Solutions

In an era of technological advancement, and easy access to such disruptors, pharmaceutical organizations are increasingly looking to outsource their solutions to enhance efficiency and reduce cost. Inevitably, there are many benefits to Regulatory Compliance Outsourcing in the pharmaceutical industry that include operational control, faster time-to-market, increased flexibility & revenue, quality production and ultimately lead

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DDReg attends National Conference on Pharmacovigilance and Clinical Research 2022

DDReg attends National Conference on Pharmacovigilance and Clinical Research 2022- Chandigarh College of Pharmacy

Drug abuse has gradually become an increasing issue due to the use of non-medical prescription drugs. Thus, pharmacovigilance and drug safety has become an even more crucial aspect for ensuring patient safety by monitoring adverse drug reactions and evaluating the safe use of medicines. To do this, robust procedures must be established while keeping in

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Nanobodies vs Antibodies

Nanobodies vs Antibodies in the Fight Against Covid

Nanobodies are engineered small proteins that recognize and specifically bind to an antigen to initiate an appropriate signal- like antibodies. However, nanobodies bind to antigens with greater specificity and display other advantages over conventional antibodies. Extracted from camelids, these antibodies were found to comprise only of heavy chains, while demonstrating the same functions as conventional

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