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Zoho Creator for Pharma: Custom Apps Building for Drug Lifecycle Management

Zoho Creator for Pharma: Custom Apps Building for Drug Lifecycle Management

Precision compliance along with business agility are hallmarks of success for a pharmaceutical organization. Drug lifecycle management is not just a convoluted process; it is a highly regulated element of a drug’s discovery to post-market surveillance. Each stage entails accurate data, secure collaboration, and regulatory standards, which makes it imperative for the right digital tools to be available.

 

Most, if not all, of such companies will use old-fashioned software or just off-the-shelf ones, which, obviously, do not attend to the ever-evolving and specialized requirements that the industry demands. That's because pretty soon, it will be found in the revolutionary world of Zoho Creator, the powerful low-code application development platform, meant for pharmaceutical organizations to develop custom, scalable, and compliant applications for streamlining the entire life cycle of drugs.

 

 Comprehending Drug Lifecycle

This drug lifecycle comprises some important stages:

  1. Discovery and Preclinical Research
  2. Clinical Trials (Phase I-III)
  3. Regulatory Approval
  4. Manufacturing and Quality Control
  5. Distribution and Supply Chain Management
  6. Post-marketing Surveillance (Pharmacovigilance)

 

All of these stages generate huge amounts of data, require collaboration of cross-functional teams, and must adhere to regulatory frameworks, such as FDA 21 CFR Part 11, GxP, ICH-GCP, and the regional health authorities. Too costly delays, haphazard data, or even violations of compliance may occur from haphazard tracking of these processes or leaving them open to different isolated systems.

 

The Zoho Creator Advantage

 

Zoho Creator is a low-code platform that enables users to build fully customized apps to their organization-specific workflows—without possessing software engineering skills. From drag-and-drop tools, templates, to a power back-end, it greatly reduces the time and cost to develop an app.

 

Here is why Zoho Creator is great for pharmaceutical companies:

 

  • Customization: Applications that fit your exact processes rather than forcing you to fit your work into a generic system
  • Scalability: Expand features or modules according to your need as your business and regulatory requirements change
  • Security & Compliance: Built-in features like audit trails, role-based access, encryption, and e-signature integration ensure meeting what the industry demands
  • Integration: Connect easily with all your existing ERP, CRM, LIMS, or 3rd party applications using APIs
  • Mobility: Access and manage on the go through mobile-friendly applications.

Let us discover how Zoho Creator supports each stage of the drug lifecycle:

  1. Drug Discovery & Preclinical Research

At the earliest stages of drug development, researchers manage massive amounts of data, such as compound libraries, assay results, toxicity profiles, and studies in animal models. Conventional spreadsheets can hardly meet such needs spanning across teams.

With Zoho Creator, pharma teams can:

  • Create a centralized database of compound and study data
  • Develop dashboards to monitor R&D progress
  • Track preclinical experiments, timelines, and resources
  • Set automated alerts for experiment milestones or pending reviews.

 

You can even integrate Zoho Creator with lab equipment or ELNs (Electronic Lab Notebooks) to pull in real-time data.

  1. Clinical Trials Management (CTMS)

Clinical trials emerge as one of the most complex and expensive phases of the drug life cycle. Managing everything from patient recruitment to adverse event tracking and maintaining compliance, every single detail counts.

 

With Zoho Creator, clinical operations can:

  • Manage protocol documents, IRB approvals, and amendments
  • Track enrollment, visit schedules, and site performance
  • Record and monitor adverse events and serious adverse events (SAEs)
  • Automate the submission of regulatory documents and track correspondence
  • Set permissions for sensitive patient data ensuring secure access by role.

You can also create an app that integrates with ePRO (electronic patient-reported outcomes) and EDC (electronic data capture) tools to build a complete CTMS.

  1. Regulatory Affairs

Compliance with regional and global regulation hinges on the effective management of submission timelines and communications with authorities for status updates across markets. This is a mammoth task.

Using Zoho Creator, regulatory teams can:

  • Maintain a centralized repository of all regulatory submissions
  • Track submission timelines, approval status, and country-specific requirements
  • Set up workflow automation for periodic safety update reports (PSURs), renewals, or changes
  • Generate reports for compliance audits
  • Receive automated alerts about imminent deadlines or document expirations.

 

The system can also record correspondence with health authorities like the FDA, EMA, or PMDA-for transparency and accountability

  1. Manufacturing & Quality Control

Since manufacturing in pharma must comply with rigorous Good Manufacturing Practices (GMP) and quality standards, paper-and-ink records or legacy systems can delay production and even create threats.

Zoho Creator apps can allow manufacturing teams to:

  • Track batch records, production runs, and inventory usage
  • Record and manage deviations, non-conformances, and CAPAs (Corrective and Preventive Actions)
  • Schedule and monitor equipment calibration and maintenance
  • Digitize and manage SOPs and ensure compliance through training logs
  • Integrate with IoT sensors for environmental monitoring (e.g., temperature, humidity)

 

Plant managers and QA heads can get real-time insights from operational performance and compliance metrics dashboards.

 

  1. Supply Chain and Distribution Management

 

This is high-stakes strategy at its best–after a drug gets approved, distribution has to be managed. The stakes become even higher when management moves inside cold chain products such as vaccines and biologics.

 

With Zoho Creator, logistics and supply chain teams can:

 

  • Monitor inventory levels and conditions in warehouses for shipment tracking routes
  • Create apps with barcode or QR code tracking for Serialized Product Tracking
  • Automate documentations and customs requirements for shipping.
  • Track returns, recalls, and conduct investigations on product complaints
  • Develop dashboards to view there are days to deliveries, vendors’ performance, and shipping costs.

 

Moreover, Zoho Creator apps can easily integrate with third-party logistics providers or fleet tracking tools.

 

  1. Postmark Surveillance (Pharmacovigilance)

 

After all, it’s not because a drug has become available that safety surveillance stops. The regulators prepare for and continue the collection of information on adverse reactions and effectiveness in the real world

 

Zoho Creator makes pharmacovigilance efficient with the following features:

 

  • Capture Adverse Drug Reactions (ADRs) from healthcare providers and patients
  • Automated case processing and categorization (serious/non-serious).
  • Report generation for regulatory submission (e.g. MedWatch, EudraVigilance).
  • Trend analysis dashboards to detect signal patterns
  • Workflow automation for investigation, escalation, and resolution of safety issues.

 

Conclusion: Agile, Compliant, and Scalable

 

In a very regulated and very innovation-driven industry like pharmaceuticals, agility and compliance are not up for negotiation. Often that means compromising feature, usability, or cost with off-the-shelf solutions. For pharmaceutical companies, Zoho Creator ensures they get the best of both worlds: custom built apps tailored to their workflows, and a secure, compliant platform that grows with them.

 

Whether you are a biotech startup managing its very first clinical trial, or you’re a multinational that is scaling operations across geographies, Zoho Creator provides the power and flexibility to optimize drug lifecycle management-ultimately accelerating time-to-market and improving patient outcomes.

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