Intelligent Enterprise

When there are enterprises catching up on the Digital Transformation, the next disruption that enterprises to be geared up is on the topic ” Intelligent enterprises”

What is Intelligent Enterprise?

There are many definitions, but simple way for me to understand is that organization which are utilizing emerging technologies like Artificial Intelligence  (AI), Machine Learning ( ML) and Internet of Things( IOT) to help their business/customer/Product to focus on the High value tasks.

There are many case studies which are emerging and when i have not witnessed anything in person but i am reading about the Robotics used in the Internal movement of goods without any Human intervention. It is like a Point to Point movement of goods with automated signals. Example: A kanban Push / Pull mechanism can be fully automated when the Bins Trigger Full/ Empty signal.


Imagine if an enterprise can provide information to the customer during the complete life cycle from order Placement till delivery of goods and also monitoring the product/service Post delivery. In case if you can also provide flexibility to modify few characteristics during intermittent Stages. I trust then the customer is going to have new experience and the enterprise will also be able to add more value to the product and serivice. If so much flexibility is required then there is lot to be improved in terms of automation, for which adapting the AI,ML,IOT all needs to be colloborated.

I will continue to explore and update this topic. If you have any practical working scenarios will be glad to connect with you.

For more information you can read here https://www.sap.com/india/products/intelligent-enterprise.html

Variant Configuration – Formal Parameter not valid

Error Message: E28086 Formal parameter MATERIAL_XX not valid for: ZVC_XXX_YYY (Line 1)

Generally to read a value from the table we will define the C’stics from table and the C’stics from the class.


On LHS= we will be giving the Table Characteristics value

and on RHS = We will be giving the value from the Variant class.

In case if you are maintaining a DB link to the VC table, then more attention to be given to the C’stics when procedure is created.

Here you should ensure that we are giving the C’stic value from the Class and not the table. If we make any mistake then the Error E28086 bound to Happen.

SAP-Roles and Authorisation- Session 3

Design to Deployment – is discussed in this video. This is the Session 3, do watch the previous 2 session which help you to catch you up for the complete details.

I was super excited to hear some feedback that these sessions are helping people to make impact on their current role and some of the feedback that i received are below.

Very Nice and thoroughly understood session Satheesh Sir .

Very helpful input in daily issue solving .

Sir , Wonderful demo . I have  now clear idea about Whats Role , How to validate it . How to search T codes from Roles. What is the functionality of authorization Object or Permission type . How to search authorization Object based on T codes using T code- Su24 .


In case if you missed my  previous session do Click below and will request you to watch in series for Better understanding and clarity.
Do watch and do leave your comments,  i will be super motivated and will keep pushing to address your requirements. Write me at [email protected] in case if you like to write any specific topic.

What is GxP?

In this Post we will look in to the GxP. This is common term as part of the compliance if we are working in any Life sciences industry.

What is GxP?

GxP is a group of compliance that the particular industry should adopt as part of the industrial / audit compliance.

G- Stands for Good
x- is  Kind of Variable.
P-stands for Practice

we will see in detail few of the X- which the life science industry adapts.


Good Manufacturing Practice:

This process details the manufacturing process and also the process that are followed to eliminate the Risk.The industry need to adopt/ publish the quality standards that it will be following.It also describes the minimum deviation.  for more info

Good Laboratory Practice.

This process details and defines the quality system for the laboratory. This applies to non clinical studies.One of the core objectives is to ensure and promote the safety and reliablility of chemical in non-clinical and laboratory testing. ..read more

Good Documentation Practice:

This process defines the standards on which the documents are created,stored and retrieved in the complete life cycle of the process.It needs to have permanent traceable records.for more info

Good Clinical Practice.

This practice  defines on the process defined to conduct the clinical trial on the human bodies.High standards are required for clinical protocol. Read more