Industry Update – AI Webinar – Why 95% of AI Pilots Fail & How the 5% Succeed


FABA (Federation of Asian Biotech Associations) US Chapter is hosting a webinar on CRACKING THE AI TRUST CODE in association with Colaberry Inc.

About the Program: Discover why 95% of AI initiatives fail and what drives the 5% that succeed.

Speakers :
1. Mr.Ram Dhan Yadav Katamaraja, Founder & CEO, Colaberry Inc
2. Dr.Ramkumar Kuncha, CEO, Arka Mark Ventures
3. Dr.Chaithanya Bandi, Professor, Kellog School of Management

Who should Attend: Researchers, Innovators, and emerging Professionals shaping the next era of intelligence.

Date , Time : Saturday, June 06, 2026; 10 :30 – 11.30AM IST , 10:00 – 11:00PM PST

Webinar Mode : Zoom meet

Registration Link: https://bit.ly/4o4R6Rk


All are requested to register and join Dr. Ramdhan and expert panelists to explore trusted AI, Agentic systems, and enterprise transformation.

NABH MITRA PROGRAM – Launch

The NABH MITRA Empanelment Programme has been officially launched to build a nationwide network of verified professionals and organisations (“MITRAs”) who will support hospitals with NABH Accreditation, Certification, and digital health transformation, especially across Tier 2, 3, and 4 cities in India.

The last date to submit applications for empanelment is October 10,2025

About the Programme

The initiative offers a structured, transparent framework for MITRAs—trusted companions to hospitals—who will guide healthcare organisations through quality improvement and digital enablement in line with NABH standards. Empanelled MITRAs will be listed on the NABH website with verified credentials and areas of expertise.

Categories of MITRAs

Digital MITRA: Supports hospitals in implementing NABH Digital Health Standards and IT enablement through structured digital health consultancy. Digital MITRA category has additional training and experience requirements

Organisational MITRAs: Support hospitals for both Full Accreditation and Entry-Level Certification.

Individual MITRAs: Independently support hospitals mainly for Entry-Level Certification.

Who Can Apply:

Individual MITRAs: Qualified professionals with at least one successful accreditation or certification support project and one NABH-certified professional (current assessors not eligible).

Organisational MITRAs: Registered companies, LLPs, trusts, societies, or proprietorship entities operational for at least one year, with experience supporting minimum three hospitals through accreditation or certification. Must have at least two NABH-certified professionals (current NABH assessors not eligible).

Application Process & Fees

i. Apply via the NABH online portal by October 10, 2025.
ii. Shortlisted candidates will be invited for interviews and required training.
iii.Empanelment fee for a three-year period: ₹20,000 + GST (Individual MITRA), ₹50,000 + GST (Organisational MITRA).
iv.Training program charges: ₹25,000 + GST for MITRA, ₹15,000 + GST for Digital MITRA (paid after selection)

Additional Information

i. MITRAs will play a key role in enabling hospitals to achieve NABH standards and strengthen India’s healthcare quality framework
ii. Empanelment does not imply endorsement or financial association by NABH.
iii.Maintaining high standards, transparency, and ethical conduct is compulsory.

Source: https://portal.nabh.co/Announcement/MEP_Concept.pdf

Workflows in the Age of AI Agents

Agent-based artificial intelligence is considered as the next leap in productivity. The logic is simple viz., assign a task to an agent and let it run. Yet the effectiveness of these systems depends far less on the sophistication of the code and far more on the clarity of the workflow they are given.

A workflow is the structured path through which work moves from start to finish. It defines the sequence of tasks, the hand-offs between people or systems, and the expected outcomes at each stage. Within this path, the process provides the backbone, setting out how each step should be performed, what standards apply, and how exceptions are to be managed. Without these foundations, the very data that agents rely on becomes unreliable. It is like attempting a Six Sigma project without stabilising the process first, because what you are measuring is so inconsistent that any optimisation is built on sand.

This is easy to see in practice. Consider a hospital admission workflow, which involves multiple departments, sensitive data, and critical timing. The journey begins with patient registration, where details are collected, a unique identity is created, and basic documentation such as identification or insurance papers is checked. The next vital step is financial clearance, either through insurance verification or collection of a deposit. If this is skipped or handled late, problems cascade downstream. Once financial clearance is complete, a medical assessment follows, triaging emergencies and routing others for physician review. Bed or room allocation then takes place, coordinated with housekeeping and transport to ensure readiness. Finally, clinical onboarding begins, with nurses briefing the patient, scheduling diagnostics, and updating the treating doctor through the hospital’s systems. From here, care and monitoring continue in a loop of data collection and coordination.

When this workflow is carefully mapped, each step is clear, responsibilities are defined, and the information flow is reliable. Insurance clearance cannot occur after room allocation, because the order is already locked. Registration cannot skip details, because every downstream task depends on them. The mapping creates discipline and ensures that the process holds together.

It is only on this foundation that AI agents add real value. They can automatically verify insurance coverage, trigger alerts when financial clearance is delayed, schedule diagnostic tests in line with physician orders, or update records in real time. But if the underlying workflow is inconsistent for instance, if insurance checks sometimes happen before and sometimes after admission the agent merely accelerates the inconsistency. Instead of solving the problem, it makes it worse.

The same logic applies to outside hospitals. In employee onboarding, for instance, the workflow may run from offer acceptance to first-day orientation, but unless the processes are consistent—laptop provisioning, payroll activation, mandatory training—the onboarding experience becomes fragmented, and any attempt to automate simply multiplies the unevenness.

AI agents are not shortcuts. They are multipliers. They multiply the clarity of a well-mapped workflow and the strength of well-defined processes. But they also multiply the confusion where structure is missing. The real question for organisations is not what agents can do, but whether the workflows and processes in place are clear enough for them to succeed.

The relevance and importance of this becomes even more clear on a ready of the article in McKinsey. They argue that productivity gains do not come from redrawing the structure chart but from rethinking the process itself. Their framework of four levers eliminate, synchronize, streamline, and automate offers a practical way to make workflows more resilient and effective. The traditional disciplines of process mapping and standardisation, sometimes dismissed as dated, are in fact more critical than ever in the age of AI agents. To eliminate is to cut away what is redundant, whether duplicate reports, excessive meetings, or unnecessary checkpoints. To synchronize is to ensure that information flows across boundaries without delay, so that decisions are taken in context and in time. To streamline is to reduce clutter, focusing on what matters most to decision quality instead of drowning people in backward-looking commentary or irrelevant granularity. And to automate is to use digital tools to take over routine work, allowing human judgment and creativity to come to the fore.

Placed against the earlier examples, the relevance is obvious. In hospital admissions, eliminating unnecessary checkpoints, synchronising across clinical and financial functions, streamlining reporting to focus on patient readiness, and automating insurance checks would not only reduce errors but also accelerate outcomes. In employee onboarding, the same four levers would prevent duplication, improve hand-offs, and allow AI agents to truly enhance the experience rather than amplify confusion.

Seen this way, the emphasis on process is not old-fashioned bureaucracy but the very foundation of modern productivity. AI becomes a companion rather than a replacement. It multiplies whatever exists discipline or disorder and the responsibility lies with organisations to ensure that what exists is well designed. Only then can agents elevate performance, reduce wasted effort, and create sustainable value.

Industry Information update : Sector-wise Compendiums of Indian Standards

BIS Unveils 130 Sector-wise Compendiums of Indian Standards to Enhance Industry and Consumer Awareness

The Bureau of Indian Standards (BIS) has released a comprehensive collection of 130 sector-specific compendiums of Indian Standards, now accessible on the BIS portal.

Organized by industry sectors and product/service categories, these compendiums serve as consolidated reference guides for a wide range of stakeholders, including regulatory authorities, industry professionals, academic institutions, and consumer organizations.

Stakeholders can access the compendiums at
https://services.bis.gov.in/php/BIS_2.0/bisconnect/compendium_of_indian_standards_dept_wise

Please scan the QR code given below to download :

Source: https://services.bis.gov.in/php/BIS_2.0/bisconnect/compendium_of_indian_standards_dept_wise

Industry Information Update – BIS – Sector wise Calendar for Upcoming Webinars

Bureau of Indian Standards is organising Sector specific awareness programs

In order to spread the awareness among the concerned stakeholders, manufacturers, importers and common consumers BIS is organising ‘Interactive lecture series and Sector-wise webinar’ on the below mentioned topics.

Manufacturers including MSMEs are requested to attend the above webinars based on their respective business interests for a particular sector.

Participation in these webinars does not require any preregistration and can be joined conveniently and remotely through Computer / Laptops / Mobiles.

The link for joining these webinars are hosted well in advance on BIS Website: www.bis.gov.in

Source: https://www.bis.gov.in/

Industry Update – Application Process for Seeking Extension of Schedule M

The Central Drugs Standard Control (CDSCO) has issued a Circular on 24th March 2025, that an online portal ONDLS has been launched for submission of application for extension of the timeline to comply with Schedule M by Small and Medium Manufacturers.

Small and Medium manufacturers with turnover of less than Rs.250 crores, can submit an application within 3 months of this notification in Form A (plan of upgradation) to the Central License Approving Authority for extension of implementation till 31st December 2025.

In this regard, CDSCO has developed an online system for submiting application through ONDLS portal.

The applicant / manufacturer seeking extension of the timeline has to register on the ONDLS portal and thereafter submit an application.

No hard copy of the application for seeking extension will be considered.

Circular of CDSCO is given below :

Source: https://statedrugs.gov.in/SFDA/ondls-login.html

Industry Update – Legal Metrology (Packaged Commodities) Rules, 2011 with amendments

The Ministry of Consumer Affairs, Food, and Public Distribution, Department of Consumer Affairs has issued The Legal Metrology (Packaged Commodities) Rules, 2011 with all amendments up to December 24, 2024.

It outlines the regulations for pre-packaged commodities in India, ensuring that consumers receive accurate information about the products they purchase. 

The rules apply to packages intended for retail sale but exclude certain categories such as:
(a) packages of commodities containing quantity of more than 25 kilogram or 25 litre
(b) cement, fertilizer and agricultural farm produce sold in bags above 50 kilogram
(c) packaged commodities meant for industrial consumers or institutional consumers

The document includes several key amendments to the Legal Metrology (Packaged Commodities) Rules, 2011, compared to earlier versions. ​ Here are some notable amendments:

  1. Consumer Definition Update:
    • The definition of “consumer” has been updated to align with the Consumer Protection Act, 2019. ​
  2. E-commerce Provisions:
    • Definitions for “E-commerce,” “E-commerce entity,” and “marketplace-based model of e-commerce” have been added. ​
    • E-commerce entities must ensure that mandatory declarations are displayed on their digital platforms. ​
  3. Retail Sale Price (MRP):
    • The format for declaring the maximum retail price has been standardized to ensure clarity and consistency. ​
  4. Unit Sale Price:
    • The requirement to declare the unit sale price in rupees, rounded off to the nearest two decimal places, has been introduced. ​
  5. QR Code Usage:
    • For electronic products, the use of QR codes to provide additional information such as the manufacturer’s address, common or generic name, and size/dimensions has been allowed. ​
  6. Packaging Size and Weight:
    • Specific packaging sizes for various commodities have been updated or added, such as for baby food, biscuits, edible oils, and more.
  7. Exemptions:
    • New exemptions have been introduced for certain packages, such as those containing loose commodities ordered through e-commerce channels and garments sold in loose or open form at the point of sale. ​
  8. Inspection and Testing:
    • Detailed procedures for inspecting and testing packages at the premises of manufacturers, packers, and dealers have been specified, including the use of statistical methods to determine compliance. ​
  9. Penalties and Compounding of Offenses:
    • The penalties for non-compliance have been updated, including specific fines for different types of offenses. ​
    • The sum for compounding offenses has been specified, with different amounts for retailers, wholesale dealers, manufacturers, and importers. ​
  10. Registration Requirements:
    • The process for registering manufacturers, packers, and importers has been clarified, including the requirement to provide a complete address and the option to register a shorter address. ​
  11. Declaration of Quantity:
    • The rules for declaring the net quantity of commodities have been refined, including the requirement to exclude the weight of wrappers and materials other than the commodity. ​
  12. Best Before/Use by Date:
    • The requirement to declare the “best before” or “use by” date for commodities that may become unfit for human consumption after a period of time has been emphasized. ​

These amendments aim to enhance consumer protection, ensure transparency, and adapt to the evolving marketplace, including the rise of e-commerce.

The e book of  Legal Metrology (Packaged Commodities) Rules, 2011 can be downloaded from https://doca.gov.in/lm-ebook/

source: https://doca.gov.in/lm-ebook/

Industry updates: Webinar on Export of Environmental Services to Argentina and Brazil

Service Export Promotion Council (SEPC) is inviting participation from the industry in Webinar on Export of Environmental Services to Argentina and Brazil. Friday, 7-Feb- 2025 4:30PM to 6:00PM IST (8:00AM to 9:30AM BRT/ART)*

Embassy of India in Argentina and Brazil will be addressing the industry stakeholders of Environmental services sector

This exercise aims to strengthen the commercial ties between the industry members of both the countries promoting Indian exports in environmental sectors through dialogue, knowledge exchange and generation of strategic action plan for 2025-26.

Topics covered :

a.Investment opportunities in Brazil for Indian Environmental consultants.
b.Any specific challenge in exporting to Brazil.
c.Any specific competence of Indian workforce required to compete in Brazil.
d.Suggest international fairs, expos, or virtual platforms for participation in Brazil.

Program highlights :


▪Valuable insights into emerging opportunities and challenges in Environmental sector.
▪Opportunity to interact with distinguished speakers from the Embassies of both the countries.

This event is set to be a platform for the exchange of ideas and the development of cooperation strategies in this sector, consolidating India’s role as a strategic partner in Their economic sphere.

Program Date & Time

Date: February 7th, 2025
Time: 4:30 PM – 6:00 PM (IST) | Platform: Online

Registration :

Click the link below for Registration
https://docs.google.com/forms/d/e/1FAIpQLSePLIyR4RkvS4eaq7F4QclQtumFhsvwUT98mkB8aUfIng8hBA/viewform?usp=mail_form_link

For more Details, please contact

Mr. Deepak Kumar Verma 8178262474 verma.deepak@servicesepc.org
Ms. Manisha Gosain 9810796729 manisha.gosain@servicesepc.org

Source: https://www.servicesepc.org/upload/Forthcoming_Event/Circular%20Environmental%20Services%20Webinar_9619.pdf

Industry Update – “MEDTECH QUALITY CHAMPION AWARDS”

MEDTECH QUALITY CHAMPION AWARDS is announced by Andhra Pradesh Medical Technology Zone (AMTZ) in collaboration with CII-Institute of Quality to facilitate organisations in the area of Quality, Innovation and Excellence.

The awards have four categories to encourage Quality initiatives with Med tech industries to meet the goal of achieve Atmanirbharta and achieve the goal of Government of India towards “Viksit Bharat-2047”.

About the Award

The MedTech Quality Champion Award recognizes and honors medical device organizations that demonstrate exceptional innovation, quality, and commitment to advancing healthcare through their products and services. This initiative not only aims to celebrate achievements but also to inspire a culture of excellence, driving organizations toward higher standards of quality and innovation.

Categories of Awards

The awards are divided into four categories:

  1. Micro and Small-Scale Enterprises
  2. Medium Enterprises
  3. Large-Scale Enterprises
  4. Service Sector Organizations

Eligibility Criteria

– Must be a legal entity in India with a minimum establishment of 2 years.
– Demonstrated a case study with application of Quality Tools & methodologies
– Relevant work completed within the last 2 years

Application Timelines

Last date for receipt of Application – 13th November 2024
Presentation by Companies – 19th to 21st November 2024
Award announcement – 27th November 2024

Visit www.cii-iq.in to download the application form and email to nidhi.barve@cii.in and karthik.v@amtz.in to submit your registrations

Award Presentation

Winners will be recognized at the CII Excellence Summit on 27 – 28 November 2024, attended by industry leaders and experts, fostering a spirit of collaboration and innovation in the MedTech sector.

Contact Details:

Nidhi Barve
Counsellor – Institute of Quality
nidhi.barve@cii.in
+91-9967950770

Karthik Raj V
Scientist B, AMTZ
karthik.v@amtz.in
+91-96771 63469

Source:
https://cii-iq.in/
https://www.amtz.in/

Industry Update – Bioenablers: Biomanufacturing Hubs 

Department of Biotechnology, Govt of India and  Biotechnology Industry Research Assistance Council (BIRAC) , jointly invite proposals for seeking support to establish Bio-Enabler: Biomanufacturing Hubs

About the Proposal

Enabling Access to Infrastructure and Resources [Bio-foundries] for Bio-manufacturing

Recognizing the potential of Biomanufacturing to power green growth, the Department of Biotechnology (DBT), Govt. of India has undertaken an initiative on Fostering High Performance Biomanufacturing.Against this backdrop, Biotechnology Industry Research Assistance Council (BIRAC), a PSU under the aegis of DBT, invites proposals from Industries/ Academic Institutes/ Incubators etc. to set up biomanufacturing hubs.

The proposals are envisaged in the Public Private Partnership (PPP) mode with financial co-sharing to co-develop integrated infrastructure (bio-foundries) including automation,workflows, processes, scale up facilities and related resources for access by start-ups andresearch communities engaged in biomanufacturing.

Key Features of the Call

Proposed facilities will support process innovation for rapid design and testing of organisms and scale-up engineering to accelerate biomanufacturing processes in the sectoral areas including but not limited to: functional foods and smart proteins, bio-based chemicals and enzymes, precision bio therapeutics, climate change and resilient agriculture, carbon capture and utilization, futuristic marine and space research.

Who can Apply?

The proposals can be submitted by Companies established under the Companies Act 2013/ The Limited Liability Partnership (LLP) incorporated under the Limited Liability Partnership Act,2008/ Academic Research Institutes, Universities, Research Foundation, Medical Colleges and Institutes – both public and private who are valid legal entities such as Trust, Society or established under central or state statute, Recognised Incubators. Applications from academia proposing facilities to be located in institutes premises should mandatorily have an industry collaborator who should operationalize and run the facility.

How to apply?

Proposals for the Scheme is required to be submitted online only. To submit a proposal online, please log on to the BIRAC website (www.birac.nic.in).

 No Hard Copy to be submitted. Proposals submitted online only would be considered.

Last date for Submission of Proposals : 04th November 2024( 5:30 p.m.)

Details of the scheme including eligibility requirements, categories for proposal submission; guidelines for support as grant and loan; agreement templates etc. are available at www.birac.nic.in

𝗟𝗮𝘀𝘁 𝗱𝗮𝘁𝗲 𝗳𝗼𝗿 𝘀𝘂𝗯𝗺𝗶𝘀𝘀𝗶𝗼𝗻:

The last date for submission of proposals under Bioenablers: Biomanufacturing Hubs is extended till 4th November 2024 (till 5.30 PM). Those who have already submitted the proposal need to revise as per the specific guidelines and revised proposal format

Source: https://www.birac.nic.in/desc_new.php?id=1144