Information technology

Information Technology allows organizations to work more efficiently and assists to maximize productivity. The major advantages include protection of records, faster communication and electronic storage. Pharmaceutical IT services can be used by companies ranging from small scale to large scale and help to overcome the challenges of drug development. With the advent of Pharmaceutical ERP Software, it has become easy to manage your business more efficiently. Pharmaceutical Software solutions can be implemented quickly and also helps industries to fulfil requirements effectively. They have the power to enhance product quality. Information Technology enables better decision-making and Pharma people have visibility to real-time & accurate information.

CUSTOMER CENTRICITY ON SOCIAL MEDIA

ARE THERE LESSONS FOR PHARMA FROM OTHER INDUSTRIES?

Imagine checking into a hotel late in the night but not being able to get the room you had so carefully chosen because the call centre didnt align with the hotel on the specification Customers in such scenarios find themselves at a loss for venting out their frustration and social media seems a good refuge Industry specific review portals and socia...

IOT AND AI CREATE ‘SMART’ DIGITAL ASSISTANTS

OPENING NEW POSSIBILITIES FOR DRUG DEVELOPMENT

was the year where pharma realised that Big Data could dramatically increase the value of data produced during drug development or coming from Electronic Medical Records EMRs and medical devices In it became clear that AI technologies could unlock much of the value of Big Data is the year where we have everything in our hands to leverage Big Dat...

Creating Better Clean Label Soft Gels Without Gelatin Crosslinking

Soft gels also known as soft capsules or soft caps are a highly popular pharmaceutical and nutraceutical dosage form with around units consumed every second globally A forecast by HJR Research predicts a CAGR of per cent over the next decade with the global market value expected to reach billion by During the same period the AsiaPacific region...

R&D DATA HUB

Breaking Silos to Enable Analytics

Traditionally controlled trials have dominated drug development Increasing focus on rare diseases and access to relevant patients have led to challenges where no single dataset can fulfil all research and development requirements Biopharmaceutical companies need to prioritise their business questions and map them to the appropriate source Construct...

Take a Pass on the 3pm Samples

Gone are the days when chemists would wait patiently for paper reports on their particular sample results to be sent to them The introduction of informatics technology brought with it results that can be delivered by email and uploaded through a central system or stored in the cloud so that they could be presented quickly and allow for timely decis...

Cost effective Data Operations

The need for an E2E data standards ecosystem

The main focus of Data Operations groups within biopharmaceutical companies is to ensure the highest possible quality of data for clinical studies With the combined challenges of compliance to Data Standards increasing diversity of data collection tools nearreal time visualisation of safety data and the opportunity of insilico studies Data Operatio...

Electronic FDA Submissions

Is APAC prepared for the 2017 mandate?

Two pieces of US legislation impact the future of the life sciences industry the Food and Drug Administration Safety and Innovation Act FDASIA and the Affordable Care Act also known as Obamacare FDASIA establishes user fee acts brings generic drugs under a stronger set of guidelines and sets into motion a countdown to May when all submissions to t...

Emerging Trends in Functional Service Outsourcing

Functional service has been ranked high among the buzz words of the clinical research industry Both sponsor organisations and service providers are equally excited about the opportunities this model offers and the potentially winwin situation it provides to them Sponsor organisations typically send individual protocolrelated service RFPs request fo...

Quality by Design

A rapid and systemic approach for pharmaceutical analysis

Quality by design QbD is defined in ICH Q R guidelines as a systematic approach to pharmaceutical development starting with predefined objectives with an emphasis on product and process understanding control Within the pharmaceutical industry there is increasing discussion about the principles of QbD analytical methods For many years analysts used...

Microsoft

Digital Pharma Initiative

Today life sciences companies around the world find themselves at difficult crossroads While research and development RD spending continues to grow drugs that actually make it to market are mired in a decadelong decline The reasons are numerous and complex Driven by more stringent government mandates aimed at protecting consumer safety and informat...

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